U.S. flag

An official website of the United States government

nsv7098710

  • Variant Calls:11
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 194 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):173,996,428-173,996,428Question Mark
    Overlapping variant regions from other studies: 194 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):173,996,439-173,996,439Question Mark
    Overlapping variant regions from other studies: 185 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):174,566,613-174,566,613Question Mark
    Overlapping variant regions from other studies: 185 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):174,566,617-174,566,617Question Mark
    Overlapping variant regions from other studies: 143 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):175,403,232-175,403,232Question Mark
    Overlapping variant regions from other studies: 143 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):175,403,232-175,403,232Question Mark
    Overlapping variant regions from other studies: 115 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):106,855,079-106,855,079Question Mark
    Overlapping variant regions from other studies: 107 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):107,431,579-107,431,579Question Mark
    Overlapping variant regions from other studies: 105 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):109,037,993-109,037,993Question Mark
    Overlapping variant regions from other studies: 123 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):112,372,417-112,372,417Question Mark
    Overlapping variant regions from other studies: 126 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):113,143,831-113,143,831Question Mark
    Overlapping variant regions from other studies: 126 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):113,143,831-113,143,831Question Mark
    Overlapping variant regions from other studies: 105 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):124,670,185-124,670,185Question Mark
    Overlapping variant regions from other studies: 105 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):124,670,185-124,670,185Question Mark
    Overlapping variant regions from other studies: 96 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):130,221,037-130,221,037Question Mark
    Overlapping variant regions from other studies: 96 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):130,221,039-130,221,039Question Mark
    Overlapping variant regions from other studies: 97 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):141,601,168-141,601,168Question Mark
    Overlapping variant regions from other studies: 97 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):141,601,169-141,601,169Question Mark
    Overlapping variant regions from other studies: 106 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):22,852,338-22,852,338Question Mark
    Overlapping variant regions from other studies: 106 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):22,852,340-22,852,340Question Mark
    Overlapping variant regions from other studies: 299 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):10,071,147-10,071,147Question Mark
    Overlapping variant regions from other studies: 299 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):10,071,149-10,071,149Question Mark
    Overlapping variant regions from other studies: 197 SVs from 37 studies. See in: genome view    
    Submitted genomic173,965,566-173,965,566Question Mark
    Overlapping variant regions from other studies: 197 SVs from 37 studies. See in: genome view    
    Submitted genomic173,965,577-173,965,577Question Mark
    Overlapping variant regions from other studies: 188 SVs from 28 studies. See in: genome view    
    Submitted genomic174,535,751-174,535,751Question Mark
    Overlapping variant regions from other studies: 188 SVs from 28 studies. See in: genome view    
    Submitted genomic174,535,755-174,535,755Question Mark
    Overlapping variant regions from other studies: 145 SVs from 19 studies. See in: genome view    
    Submitted genomic175,372,368-175,372,368Question Mark
    Overlapping variant regions from other studies: 145 SVs from 19 studies. See in: genome view    
    Submitted genomic175,372,368-175,372,368Question Mark
    Overlapping variant regions from other studies: 106 SVs from 20 studies. See in: genome view    
    Submitted genomic107,302,954-107,302,954Question Mark
    Overlapping variant regions from other studies: 107 SVs from 17 studies. See in: genome view    
    Submitted genomic107,752,783-107,752,783Question Mark
    Overlapping variant regions from other studies: 105 SVs from 22 studies. See in: genome view    
    Submitted genomic109,359,196-109,359,196Question Mark
    Overlapping variant regions from other studies: 123 SVs from 25 studies. See in: genome view    
    Submitted genomic112,693,619-112,693,619Question Mark
    Overlapping variant regions from other studies: 126 SVs from 22 studies. See in: genome view    
    Submitted genomic113,465,033-113,465,033Question Mark
    Overlapping variant regions from other studies: 126 SVs from 22 studies. See in: genome view    
    Submitted genomic113,465,033-113,465,033Question Mark
    Overlapping variant regions from other studies: 105 SVs from 19 studies. See in: genome view    
    Submitted genomic124,991,331-124,991,331Question Mark
    Overlapping variant regions from other studies: 105 SVs from 19 studies. See in: genome view    
    Submitted genomic124,991,331-124,991,331Question Mark
    Overlapping variant regions from other studies: 96 SVs from 20 studies. See in: genome view    
    Submitted genomic130,542,182-130,542,182Question Mark
    Overlapping variant regions from other studies: 96 SVs from 20 studies. See in: genome view    
    Submitted genomic130,542,184-130,542,184Question Mark
    Overlapping variant regions from other studies: 97 SVs from 22 studies. See in: genome view    
    Submitted genomic141,922,305-141,922,305Question Mark
    Overlapping variant regions from other studies: 97 SVs from 22 studies. See in: genome view    
    Submitted genomic141,922,306-141,922,306Question Mark
    Overlapping variant regions from other studies: 106 SVs from 20 studies. See in: genome view    
    Submitted genomic22,852,567-22,852,567Question Mark
    Overlapping variant regions from other studies: 106 SVs from 20 studies. See in: genome view    
    Submitted genomic22,852,569-22,852,569Question Mark
    Overlapping variant regions from other studies: 303 SVs from 32 studies. See in: genome view    
    Submitted genomic10,071,147-10,071,147Question Mark
    Overlapping variant regions from other studies: 303 SVs from 32 studies. See in: genome view    
    Submitted genomic10,071,149-10,071,149Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1173,996,428173,996,428+
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1173,996,439173,996,439+
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1174,566,613174,566,613-
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1174,566,617174,566,617+
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1175,403,232175,403,232+
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1175,403,232175,403,232-
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6106,855,079106,855,079+
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6107,431,579107,431,579-
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6109,037,993109,037,993+
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6112,372,417112,372,417+
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6113,143,831113,143,831-
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6113,143,831113,143,831-
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6124,670,185124,670,185+
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6124,670,185124,670,185-
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6130,221,037130,221,037+
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6130,221,039130,221,039-
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6141,601,168141,601,168+
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6141,601,169141,601,169-
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr622,852,33822,852,338-
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr622,852,34022,852,340+
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr910,071,14710,071,147-
    nsv7098710RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr910,071,14910,071,149+
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1173,965,566173,965,566+
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1173,965,577173,965,577+
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1174,535,751174,535,751-
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1174,535,755174,535,755+
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1175,372,368175,372,368+
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1175,372,368175,372,368-
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6107,302,954107,302,954+
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6107,752,783107,752,783-
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6109,359,196109,359,196+
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6112,693,619112,693,619+
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6113,465,033113,465,033-
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6113,465,033113,465,033-
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6124,991,331124,991,331+
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6124,991,331124,991,331-
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6130,542,182130,542,182+
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6130,542,184130,542,184-
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6141,922,305141,922,305+
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6141,922,306141,922,306-
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr622,852,56722,852,567-
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr622,852,56922,852,569+
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr910,071,14710,071,147-
    nsv7098710Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr910,071,14910,071,149+

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv18792457interchromosomal translocationFHU17-359SequencingSequence alignment11
    nssv18792458interchromosomal translocationFHU17-359SequencingSequence alignment11
    nssv18792465interchromosomal translocationFHU17-359SequencingSequence alignment11
    nssv18792459interchromosomal translocationFHU17-359SequencingSequence alignment11
    nssv18792464interchromosomal translocationFHU17-359SequencingSequence alignment11
    nssv18792466interchromosomal translocationFHU17-359SequencingSequence alignment11
    nssv18792463intrachromosomal translocationFHU17-359SequencingSequence alignment11
    nssv18792460intrachromosomal translocationFHU17-359SequencingSequence alignment11
    nssv18792462intrachromosomal translocationFHU17-359SequencingSequence alignment11
    nssv18792461interchromosomal translocationFHU17-359SequencingSequence alignment11
    nssv18792467interchromosomal translocationFHU17-359SequencingSequence alignment11

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
    nssv18792457RemappedPerfectGRCh38.p12First PassNC_000001.11Chr1173,996,428173,996,428+
    nssv18792458RemappedPerfectGRCh38.p12First PassNC_000001.11Chr1173,996,439173,996,439+
    nssv18792465RemappedPerfectGRCh38.p12First PassNC_000001.11Chr1174,566,613174,566,613-
    nssv18792459RemappedPerfectGRCh38.p12First PassNC_000001.11Chr1174,566,617174,566,617+
    nssv18792464RemappedPerfectGRCh38.p12First PassNC_000001.11Chr1175,403,232175,403,232+
    nssv18792466RemappedPerfectGRCh38.p12First PassNC_000001.11Chr1175,403,232175,403,232-
    nssv18792463RemappedPerfectGRCh38.p12First PassNC_000006.12Chr622,852,33822,852,338-
    nssv18792460RemappedPerfectGRCh38.p12First PassNC_000006.12Chr622,852,34022,852,340+
    nssv18792464RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6106,855,079106,855,079+
    nssv18792458RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6107,431,579107,431,579-
    nssv18792457RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6109,037,993109,037,993+
    nssv18792459RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6112,372,417112,372,417+
    nssv18792460RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6113,143,831113,143,831-
    nssv18792462RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6113,143,831113,143,831-
    nssv18792462RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6124,670,185124,670,185+
    nssv18792463RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6124,670,185124,670,185-
    nssv18792461RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6130,221,037130,221,037+
    nssv18792467RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6130,221,039130,221,039-
    nssv18792465RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6141,601,168141,601,168+
    nssv18792466RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6141,601,169141,601,169-
    nssv18792461RemappedPerfectGRCh38.p12First PassNC_000009.12Chr910,071,14710,071,147-
    nssv18792467RemappedPerfectGRCh38.p12First PassNC_000009.12Chr910,071,14910,071,149+
    nssv18792457Submitted genomicGRCh37 (hg19)NC_000001.10Chr1173,965,566173,965,566+
    nssv18792458Submitted genomicGRCh37 (hg19)NC_000001.10Chr1173,965,577173,965,577+
    nssv18792465Submitted genomicGRCh37 (hg19)NC_000001.10Chr1174,535,751174,535,751-
    nssv18792459Submitted genomicGRCh37 (hg19)NC_000001.10Chr1174,535,755174,535,755+
    nssv18792464Submitted genomicGRCh37 (hg19)NC_000001.10Chr1175,372,368175,372,368+
    nssv18792466Submitted genomicGRCh37 (hg19)NC_000001.10Chr1175,372,368175,372,368-
    nssv18792463Submitted genomicGRCh37 (hg19)NC_000006.11Chr622,852,56722,852,567-
    nssv18792460Submitted genomicGRCh37 (hg19)NC_000006.11Chr622,852,56922,852,569+
    nssv18792464Submitted genomicGRCh37 (hg19)NC_000006.11Chr6107,302,954107,302,954+
    nssv18792458Submitted genomicGRCh37 (hg19)NC_000006.11Chr6107,752,783107,752,783-
    nssv18792457Submitted genomicGRCh37 (hg19)NC_000006.11Chr6109,359,196109,359,196+
    nssv18792459Submitted genomicGRCh37 (hg19)NC_000006.11Chr6112,693,619112,693,619+
    nssv18792460Submitted genomicGRCh37 (hg19)NC_000006.11Chr6113,465,033113,465,033-
    nssv18792462Submitted genomicGRCh37 (hg19)NC_000006.11Chr6113,465,033113,465,033-
    nssv18792462Submitted genomicGRCh37 (hg19)NC_000006.11Chr6124,991,331124,991,331+
    nssv18792463Submitted genomicGRCh37 (hg19)NC_000006.11Chr6124,991,331124,991,331-
    nssv18792461Submitted genomicGRCh37 (hg19)NC_000006.11Chr6130,542,182130,542,182+
    nssv18792467Submitted genomicGRCh37 (hg19)NC_000006.11Chr6130,542,184130,542,184-
    nssv18792465Submitted genomicGRCh37 (hg19)NC_000006.11Chr6141,922,305141,922,305+
    nssv18792466Submitted genomicGRCh37 (hg19)NC_000006.11Chr6141,922,306141,922,306-
    nssv18792461Submitted genomicGRCh37 (hg19)NC_000009.11Chr910,071,14710,071,147-
    nssv18792467Submitted genomicGRCh37 (hg19)NC_000009.11Chr910,071,14910,071,149+

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    No genotype data were submitted for this variant

    You are here: NCBI
    Support Center