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nsv6451560

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:44,220

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 580 SVs from 73 studies. See in: genome view    
    Submitted genomic137,410,037-137,454,256Question Mark
    Overlapping variant regions from other studies: 580 SVs from 73 studies. See in: genome view    
    Remapped(Score: Perfect):140,304,489-140,348,708Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6451560Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9137,410,037137,454,256
    nsv6451560RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9140,304,489140,348,708

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18235393duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18235393Submitted genomicNC_000009.12:g.137
    410037_137454256du
    p
    GRCh38 (hg38)NC_000009.12Chr9137,410,037137,454,256
    nssv18235393RemappedPerfectNC_000009.11:g.140
    304489_140348708du
    p
    GRCh37.p13First PassNC_000009.11Chr9140,304,489140,348,708

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv18235393<0.001139258
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