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nsv6783362

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:212,340

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 749 SVs from 76 studies. See in: genome view    
    Submitted genomic26,321,412-26,533,751Question Mark
    Overlapping variant regions from other studies: 749 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):26,321,640-26,533,979Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6783362Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr626,321,41226,533,751
    nsv6783362RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr626,321,64026,533,979

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18527860deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18527860Submitted genomicNC_000006.12:g.263
    21412_26533751del
    GRCh38 (hg38)NC_000006.12Chr626,321,41226,533,751
    nssv18527860RemappedPerfectNC_000006.11:g.263
    21640_26533979del
    GRCh37.p13First PassNC_000006.11Chr626,321,64026,533,979

    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)
    nssv185278601.1e-053272836
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