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nsv6332598

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:434,881

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1200 SVs from 72 studies. See in: genome view    
    Submitted genomic99,642,179-100,077,059Question Mark
    Overlapping variant regions from other studies: 1200 SVs from 72 studies. See in: genome view    
    Remapped(Score: Perfect):100,107,735-100,542,615Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6332598Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr199,642,179100,077,059
    nsv6332598RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1100,107,735100,542,615

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18202143duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18202143Submitted genomicNC_000001.11:g.996
    42179_100077059dup
    GRCh38 (hg38)NC_000001.11Chr199,642,179100,077,059
    nssv18202143RemappedPerfectNC_000001.10:g.100
    107735_100542615du
    p
    GRCh37.p13First PassNC_000001.10Chr1100,107,735100,542,615

    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)
    nssv18202143<0.001139282
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