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nsv6902434

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,686

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 202 SVs from 51 studies. See in: genome view    
    Submitted genomic2,305,622-2,319,307Question Mark
    Overlapping variant regions from other studies: 202 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):2,326,852-2,340,537Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6902434Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr112,305,6222,319,307
    nsv6902434RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr112,326,8522,340,537

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18345572deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18345572Submitted genomicNC_000011.10:g.230
    5622_2319307del
    GRCh38 (hg38)NC_000011.10Chr112,305,6222,319,307
    nssv18345572RemappedPerfectNC_000011.9:g.2326
    852_2340537del
    GRCh37.p13First PassNC_000011.9Chr112,326,8522,340,537

    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)
    nssv183455727e-062276230
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