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nsv6870133

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,833,010

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4775 SVs from 97 studies. See in: genome view    
    Submitted genomic34,043,094-35,876,103Question Mark
    Overlapping variant regions from other studies: 4782 SVs from 97 studies. See in: genome view    
    Remapped(Score: Perfect):34,043,092-35,876,100Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6870133Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr934,043,09435,876,103
    nsv6870133RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr934,043,09235,876,100

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18569530deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18569530Submitted genomicNC_000009.12:g.340
    43094_35876103del
    GRCh38 (hg38)NC_000009.12Chr934,043,09435,876,103
    nssv18569530RemappedPerfectNC_000009.11:g.340
    43092_35876100del
    GRCh37.p13First PassNC_000009.11Chr934,043,09235,876,100

    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)
    nssv185695304e-061259198
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