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nsv6752757

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,298

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 165 SVs from 33 studies. See in: genome view    
    Submitted genomic82,884,189-82,888,486Question Mark
    Overlapping variant regions from other studies: 165 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):83,805,342-83,809,639Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6752757Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr482,884,18982,888,486
    nsv6752757RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr483,805,34283,809,639

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18500859deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18500859Submitted genomicNC_000004.12:g.828
    84189_82888486del
    GRCh38 (hg38)NC_000004.12Chr482,884,18982,888,486
    nssv18500859RemappedPerfectNC_000004.11:g.838
    05342_83809639del
    GRCh37.p13First PassNC_000004.11Chr483,805,34283,809,639

    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)
    nssv185008594e-061274716
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