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nsv6439692

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:520,672

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2057 SVs from 107 studies. See in: genome view    
    Submitted genomic4,682,156-5,202,827Question Mark
    Overlapping variant regions from other studies: 2057 SVs from 107 studies. See in: genome view    
    Remapped(Score: Perfect):4,703,386-5,224,057Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6439692Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr114,682,1565,202,827
    nsv6439692RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr114,703,3865,224,057

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18188514duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18188514Submitted genomicNC_000011.10:g.468
    2156_5202827dup
    GRCh38 (hg38)NC_000011.10Chr114,682,1565,202,827
    nssv18188514RemappedPerfectNC_000011.9:g.4703
    386_5224057dup
    GRCh37.p13First PassNC_000011.9Chr114,703,3865,224,057

    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)
    nssv18188514<0.001139296
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