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nsv6863756

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:45,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 465 SVs from 39 studies. See in: genome view    
    Submitted genomic2,622,301-2,668,200Question Mark
    Overlapping variant regions from other studies: 467 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):2,622,301-2,668,200Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6863756Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr92,622,3012,668,200
    nsv6863756RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr92,622,3012,668,200

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18566077deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18566077Submitted genomicNC_000009.12:g.262
    2301_2668200del
    GRCh38 (hg38)NC_000009.12Chr92,622,3012,668,200
    nssv18566077RemappedPerfectNC_000009.11:g.262
    2301_2668200del
    GRCh37.p13First PassNC_000009.11Chr92,622,3012,668,200

    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)
    nssv185660774e-061276030
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