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nsv6961031

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 366 SVs from 33 studies. See in: genome view    
    Submitted genomic1,316,401-1,318,500Question Mark
    Overlapping variant regions from other studies: 366 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):1,366,402-1,368,501Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6961031Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr161,316,4011,318,500
    nsv6961031RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr161,366,4021,368,501

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18398887deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18398887Submitted genomicNC_000016.10:g.131
    6401_1318500del
    GRCh38 (hg38)NC_000016.10Chr161,316,4011,318,500
    nssv18398887RemappedPerfectNC_000016.9:g.1366
    402_1368501del
    GRCh37.p13First PassNC_000016.9Chr161,366,4021,368,501

    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)
    nssv183988874e-061275326
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