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nsv6441527

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:119,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 613 SVs from 76 studies. See in: genome view    
    Submitted genomic110,190,601-110,309,700Question Mark
    Overlapping variant regions from other studies: 613 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):112,952,881-113,071,980Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6441527Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9110,190,601110,309,700
    nsv6441527RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9112,952,881113,071,980

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18235984duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18235984Submitted genomicNC_000009.12:g.110
    190601_110309700du
    p
    GRCh38 (hg38)NC_000009.12Chr9110,190,601110,309,700
    nssv18235984RemappedPerfectNC_000009.11:g.112
    952881_113071980du
    p
    GRCh37.p13First PassNC_000009.11Chr9112,952,881113,071,980

    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)
    nssv18235984<0.001337728
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