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nsv7098699

  • Variant Calls:4
  • 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: 374 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):2,587,592-2,587,592Question Mark
    Overlapping variant regions from other studies: 374 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):2,587,592-2,587,592Question Mark
    Overlapping variant regions from other studies: 195 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):92,312,271-92,312,271Question Mark
    Overlapping variant regions from other studies: 195 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):92,312,274-92,312,274Question Mark
    Overlapping variant regions from other studies: 179 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):93,005,323-93,005,323Question Mark
    Overlapping variant regions from other studies: 179 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):93,005,324-93,005,324Question Mark
    Overlapping variant regions from other studies: 114 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):55,726,540-55,726,540Question Mark
    Overlapping variant regions from other studies: 114 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):55,726,543-55,726,543Question Mark
    Overlapping variant regions from other studies: 374 SVs from 39 studies. See in: genome view    
    Submitted genomic2,629,276-2,629,276Question Mark
    Overlapping variant regions from other studies: 374 SVs from 39 studies. See in: genome view    
    Submitted genomic2,629,276-2,629,276Question Mark
    Overlapping variant regions from other studies: 195 SVs from 42 studies. See in: genome view    
    Submitted genomic93,233,422-93,233,422Question Mark
    Overlapping variant regions from other studies: 195 SVs from 42 studies. See in: genome view    
    Submitted genomic93,233,425-93,233,425Question Mark
    Overlapping variant regions from other studies: 179 SVs from 31 studies. See in: genome view    
    Submitted genomic93,926,474-93,926,474Question Mark
    Overlapping variant regions from other studies: 179 SVs from 31 studies. See in: genome view    
    Submitted genomic93,926,475-93,926,475Question Mark
    Overlapping variant regions from other studies: 114 SVs from 24 studies. See in: genome view    
    Submitted genomic56,193,258-56,193,258Question Mark
    Overlapping variant regions from other studies: 114 SVs from 24 studies. See in: genome view    
    Submitted genomic56,193,261-56,193,261Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
    nsv7098699RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr32,587,5922,587,592+
    nsv7098699RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr32,587,5922,587,592-
    nsv7098699RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr492,312,27192,312,271+
    nsv7098699RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr492,312,27492,312,274-
    nsv7098699RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr493,005,32393,005,323-
    nsv7098699RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr493,005,32493,005,324+
    nsv7098699RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1455,726,54055,726,540-
    nsv7098699RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1455,726,54355,726,543+
    nsv7098699Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr32,629,2762,629,276+
    nsv7098699Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr32,629,2762,629,276-
    nsv7098699Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000004.11Chr493,233,42293,233,422+
    nsv7098699Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000004.11Chr493,233,42593,233,425-
    nsv7098699Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000004.11Chr493,926,47493,926,474-
    nsv7098699Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000004.11Chr493,926,47593,926,475+
    nsv7098699Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000014.8Chr1456,193,25856,193,258-
    nsv7098699Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000014.8Chr1456,193,26156,193,261+

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv18792496interchromosomal translocationFHU19-162SequencingSequence alignmentnssv18792497, nssv18792498, nssv18792499
    nssv18792499interchromosomal translocationFHU19-162SequencingSequence alignmentnssv18792496, nssv18792497, nssv18792498
    nssv18792497intrachromosomal translocationFHU19-162SequencingSequence alignmentnssv18792496, nssv18792498, nssv18792499
    nssv18792498interchromosomal translocationFHU19-162SequencingSequence alignmentnssv18792496, nssv18792497, nssv18792499

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
    nssv18792496RemappedPerfectGRCh38.p12First PassNC_000003.12Chr32,587,5922,587,592-
    nssv18792499RemappedPerfectGRCh38.p12First PassNC_000003.12Chr32,587,5922,587,592+
    nssv18792497RemappedPerfectGRCh38.p12First PassNC_000004.12Chr492,312,27192,312,271+
    nssv18792498RemappedPerfectGRCh38.p12First PassNC_000004.12Chr492,312,27492,312,274-
    nssv18792496RemappedPerfectGRCh38.p12First PassNC_000004.12Chr493,005,32393,005,323-
    nssv18792497RemappedPerfectGRCh38.p12First PassNC_000004.12Chr493,005,32493,005,324+
    nssv18792498RemappedPerfectGRCh38.p12First PassNC_000014.9Chr1455,726,54055,726,540-
    nssv18792499RemappedPerfectGRCh38.p12First PassNC_000014.9Chr1455,726,54355,726,543+
    nssv18792496Submitted genomicGRCh37 (hg19)NC_000003.11Chr32,629,2762,629,276-
    nssv18792499Submitted genomicGRCh37 (hg19)NC_000003.11Chr32,629,2762,629,276+
    nssv18792497Submitted genomicGRCh37 (hg19)NC_000004.11Chr493,233,42293,233,422+
    nssv18792498Submitted genomicGRCh37 (hg19)NC_000004.11Chr493,233,42593,233,425-
    nssv18792496Submitted genomicGRCh37 (hg19)NC_000004.11Chr493,926,47493,926,474-
    nssv18792497Submitted genomicGRCh37 (hg19)NC_000004.11Chr493,926,47593,926,475+
    nssv18792498Submitted genomicGRCh37 (hg19)NC_000014.8Chr1456,193,25856,193,258-
    nssv18792499Submitted genomicGRCh37 (hg19)NC_000014.8Chr1456,193,26156,193,261+

    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

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