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nsv6643320

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:156

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 118 SVs from 24 studies. See in: genome view    
    Submitted genomic159,923,522-159,923,677Question Mark
    Overlapping variant regions from other studies: 122 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):159,893,312-159,893,467Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6643320Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1159,923,522159,923,677
    nsv6643320RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1159,893,312159,893,467

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18586160duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18586160Submitted genomicNC_000001.11:g.159
    923522_159923677du
    p
    GRCh38 (hg38)NC_000001.11Chr1159,923,522159,923,677
    nssv18586160RemappedPerfectNC_000001.10:g.159
    893312_159893467du
    p
    GRCh37.p13First PassNC_000001.10Chr1159,893,312159,893,467

    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)
    nssv185861603.8e-059233610
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