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nsv7098708

  • Variant Calls:6
  • 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: 121 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):62,710,082-62,710,082Question Mark
    Overlapping variant regions from other studies: 117 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):63,811,599-63,811,599Question Mark
    Overlapping variant regions from other studies: 259 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):14,648,286-14,648,286Question Mark
    Overlapping variant regions from other studies: 259 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):14,648,286-14,648,286Question Mark
    Overlapping variant regions from other studies: 214 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):18,390,134-18,390,134Question Mark
    Overlapping variant regions from other studies: 214 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):18,390,140-18,390,140Question Mark
    Overlapping variant regions from other studies: 200 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):20,518,298-20,518,298Question Mark
    Overlapping variant regions from other studies: 200 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):20,518,299-20,518,299Question Mark
    Overlapping variant regions from other studies: 187 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):53,690,056-53,690,056Question Mark
    Overlapping variant regions from other studies: 223 SVs from 13 studies. See in: genome view    
    Remapped(Score: Perfect):5,597,978-5,597,978Question Mark
    Overlapping variant regions from other studies: 223 SVs from 13 studies. See in: genome view    
    Remapped(Score: Perfect):5,597,984-5,597,984Question Mark
    Overlapping variant regions from other studies: 231 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):61,991,870-61,991,870Question Mark
    Overlapping variant regions from other studies: 121 SVs from 19 studies. See in: genome view    
    Submitted genomic63,175,753-63,175,753Question Mark
    Overlapping variant regions from other studies: 117 SVs from 20 studies. See in: genome view    
    Submitted genomic64,277,270-64,277,270Question Mark
    Overlapping variant regions from other studies: 265 SVs from 31 studies. See in: genome view    
    Submitted genomic14,648,284-14,648,284Question Mark
    Overlapping variant regions from other studies: 265 SVs from 31 studies. See in: genome view    
    Submitted genomic14,648,284-14,648,284Question Mark
    Overlapping variant regions from other studies: 220 SVs from 25 studies. See in: genome view    
    Submitted genomic18,390,132-18,390,132Question Mark
    Overlapping variant regions from other studies: 220 SVs from 25 studies. See in: genome view    
    Submitted genomic18,390,138-18,390,138Question Mark
    Overlapping variant regions from other studies: 206 SVs from 28 studies. See in: genome view    
    Submitted genomic20,518,296-20,518,296Question Mark
    Overlapping variant regions from other studies: 206 SVs from 28 studies. See in: genome view    
    Submitted genomic20,518,297-20,518,297Question Mark
    Overlapping variant regions from other studies: 187 SVs from 19 studies. See in: genome view    
    Submitted genomic51,216,426-51,216,426Question Mark
    Overlapping variant regions from other studies: 223 SVs from 13 studies. See in: genome view    
    Submitted genomic5,597,977-5,597,977Question Mark
    Overlapping variant regions from other studies: 223 SVs from 13 studies. See in: genome view    
    Submitted genomic5,597,983-5,597,983Question Mark
    Overlapping variant regions from other studies: 231 SVs from 16 studies. See in: genome view    
    Submitted genomic59,659,103-59,659,103Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
    nsv7098708RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr162,710,08262,710,082+
    nsv7098708RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr163,811,59963,811,599-
    nsv7098708RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr914,648,28614,648,286+
    nsv7098708RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr914,648,28614,648,286-
    nsv7098708RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr918,390,13418,390,134+
    nsv7098708RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr918,390,14018,390,140-
    nsv7098708RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr920,518,29820,518,298-
    nsv7098708RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr920,518,29920,518,299+
    nsv7098708RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr1853,690,05653,690,056+
    nsv7098708RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr185,597,9785,597,978-
    nsv7098708RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr185,597,9845,597,984+
    nsv7098708RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr1861,991,87061,991,870-
    nsv7098708Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr163,175,75363,175,753+
    nsv7098708Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr164,277,27064,277,270-
    nsv7098708Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr914,648,28414,648,284+
    nsv7098708Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr914,648,28414,648,284-
    nsv7098708Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr918,390,13218,390,132+
    nsv7098708Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr918,390,13818,390,138-
    nsv7098708Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr920,518,29620,518,296-
    nsv7098708Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr920,518,29720,518,297+
    nsv7098708Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000018.9Chr1851,216,42651,216,426+
    nsv7098708Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000018.9Chr185,597,9775,597,977-
    nsv7098708Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000018.9Chr185,597,9835,597,983+
    nsv7098708Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000018.9Chr1859,659,10359,659,103-

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv18792453interchromosomal translocationFHU17-282SequencingSequence alignment6
    nssv18792452interchromosomal translocationFHU17-282SequencingSequence alignment6
    nssv18792454intrachromosomal translocationFHU17-282SequencingSequence alignment6
    nssv18792455interchromosomal translocationFHU17-282SequencingSequence alignment6
    nssv18792451interchromosomal translocationFHU17-282SequencingSequence alignment6
    nssv18792456intrachromosomal translocationFHU17-282SequencingSequence alignment6

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
    nssv18792453RemappedPerfectGRCh38.p12First PassNC_000001.11Chr162,710,08262,710,082+
    nssv18792452RemappedPerfectGRCh38.p12First PassNC_000001.11Chr163,811,59963,811,599-
    nssv18792453RemappedPerfectGRCh38.p12First PassNC_000009.12Chr914,648,28614,648,286-
    nssv18792454RemappedPerfectGRCh38.p12First PassNC_000009.12Chr914,648,28614,648,286+
    nssv18792455RemappedPerfectGRCh38.p12First PassNC_000009.12Chr918,390,13418,390,134+
    nssv18792451RemappedPerfectGRCh38.p12First PassNC_000009.12Chr918,390,14018,390,140-
    nssv18792454RemappedPerfectGRCh38.p12First PassNC_000009.12Chr920,518,29820,518,298-
    nssv18792452RemappedPerfectGRCh38.p12First PassNC_000009.12Chr920,518,29920,518,299+
    nssv18792455RemappedPerfectGRCh38.p12First PassNC_000018.10Chr185,597,9785,597,978-
    nssv18792451RemappedPerfectGRCh38.p12First PassNC_000018.10Chr185,597,9845,597,984+
    nssv18792456RemappedPerfectGRCh38.p12First PassNC_000018.10Chr1853,690,05653,690,056+
    nssv18792456RemappedPerfectGRCh38.p12First PassNC_000018.10Chr1861,991,87061,991,870-
    nssv18792453Submitted genomicGRCh37 (hg19)NC_000001.10Chr163,175,75363,175,753+
    nssv18792452Submitted genomicGRCh37 (hg19)NC_000001.10Chr164,277,27064,277,270-
    nssv18792453Submitted genomicGRCh37 (hg19)NC_000009.11Chr914,648,28414,648,284-
    nssv18792454Submitted genomicGRCh37 (hg19)NC_000009.11Chr914,648,28414,648,284+
    nssv18792455Submitted genomicGRCh37 (hg19)NC_000009.11Chr918,390,13218,390,132+
    nssv18792451Submitted genomicGRCh37 (hg19)NC_000009.11Chr918,390,13818,390,138-
    nssv18792454Submitted genomicGRCh37 (hg19)NC_000009.11Chr920,518,29620,518,296-
    nssv18792452Submitted genomicGRCh37 (hg19)NC_000009.11Chr920,518,29720,518,297+
    nssv18792455Submitted genomicGRCh37 (hg19)NC_000018.9Chr185,597,9775,597,977-
    nssv18792451Submitted genomicGRCh37 (hg19)NC_000018.9Chr185,597,9835,597,983+
    nssv18792456Submitted genomicGRCh37 (hg19)NC_000018.9Chr1851,216,42651,216,426+
    nssv18792456Submitted genomicGRCh37 (hg19)NC_000018.9Chr1859,659,10359,659,103-

    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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