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nsv6990261

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:116,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 599 SVs from 68 studies. See in: genome view    
    Submitted genomic75,544,101-75,660,900Question Mark
    Overlapping variant regions from other studies: 599 SVs from 68 studies. See in: genome view    
    Remapped(Score: Good):73,540,182-73,656,980Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6990261Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1775,544,10175,660,900
    nsv6990261RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1773,540,18273,656,980

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18415255deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18415255Submitted genomicNC_000017.11:g.755
    44101_75660900del
    GRCh38 (hg38)NC_000017.11Chr1775,544,10175,660,900
    nssv18415255RemappedGoodNC_000017.10:g.735
    40182_73656980del
    GRCh37.p13First PassNC_000017.10Chr1773,540,18273,656,980

    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)
    nssv184152554e-061276230
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