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nsv6504534

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:611,145

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1987 SVs from 90 studies. See in: genome view    
    Submitted genomic6,527,065-7,138,209Question Mark
    Overlapping variant regions from other studies: 1987 SVs from 90 studies. See in: genome view    
    Remapped(Score: Perfect):6,430,385-7,041,528Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6504534Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr176,527,0657,138,209
    nsv6504534RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr176,430,3857,041,528

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18179546duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18179546Submitted genomicNC_000017.11:g.652
    7065_7138209dup
    GRCh38 (hg38)NC_000017.11Chr176,527,0657,138,209
    nssv18179546RemappedPerfectNC_000017.10:g.643
    0385_7041528dup
    GRCh37.p13First PassNC_000017.10Chr176,430,3857,041,528

    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)
    nssv18179546<0.001139288
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