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nsv6434081

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 148 SVs from 17 studies. See in: genome view    
    Submitted genomic101,200,601-101,205,000Question Mark
    Overlapping variant regions from other studies: 148 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):102,212,829-102,217,228Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6434081Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8101,200,601101,205,000
    nsv6434081RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8102,212,829102,217,228

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18235083duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18235083Submitted genomicNC_000008.11:g.101
    200601_101205000du
    p
    GRCh38 (hg38)NC_000008.11Chr8101,200,601101,205,000
    nssv18235083RemappedPerfectNC_000008.10:g.102
    212829_102217228du
    p
    GRCh37.p13First PassNC_000008.10Chr8102,212,829102,217,228

    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)
    nssv18235083<0.0013939258
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