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nsv6964153

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,714

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 221 SVs from 26 studies. See in: genome view    
    Submitted genomic1,677,110-1,678,823Question Mark
    Overlapping variant regions from other studies: 221 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):1,727,111-1,728,824Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6964153Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr161,677,1101,678,823
    nsv6964153RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr161,727,1111,728,824

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18621307duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18621307Submitted genomicNC_000016.10:g.167
    7110_1678823dup
    GRCh38 (hg38)NC_000016.10Chr161,677,1101,678,823
    nssv18621307RemappedPerfectNC_000016.9:g.1727
    111_1728824dup
    GRCh37.p13First PassNC_000016.9Chr161,727,1111,728,824

    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)
    nssv186213074e-061271062
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