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nsv6859850

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:365,344

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1472 SVs from 85 studies. See in: genome view    
    Submitted genomic12,353,426-12,718,769Question Mark
    Overlapping variant regions from other studies: 1476 SVs from 85 studies. See in: genome view    
    Remapped(Score: Perfect):12,353,426-12,718,768Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6859850Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr912,353,42612,718,769
    nsv6859850RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr912,353,42612,718,768

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18565580deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18565580Submitted genomicNC_000009.12:g.123
    53426_12718769del
    GRCh38 (hg38)NC_000009.12Chr912,353,42612,718,769
    nssv18565580RemappedPerfectNC_000009.11:g.123
    53426_12718768del
    GRCh37.p13First PassNC_000009.11Chr912,353,42612,718,768

    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)
    nssv185655807e-062270818
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