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nsv6612057

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:495,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3424 SVs from 102 studies. See in: genome view    
    Submitted genomic62,516,501-63,012,000Question Mark
    Overlapping variant regions from other studies: 3463 SVs from 102 studies. See in: genome view    
    Remapped(Score: Perfect):61,976,879-62,472,378Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6612057Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr762,516,50163,012,000
    nsv6612057RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr761,976,87962,472,378

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18231105duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18231105Submitted genomicNC_000007.14:g.625
    16501_63012000dup
    GRCh38 (hg38)NC_000007.14Chr762,516,50163,012,000
    nssv18231105RemappedPerfectNC_000007.13:g.619
    76879_62472378dup
    GRCh37.p13First PassNC_000007.13Chr761,976,87962,472,378

    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)
    nssv182311050.00414638584
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