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nsv6703639

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:34,523

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 251 SVs from 47 studies. See in: genome view    
    Submitted genomic236,516,074-236,550,596Question Mark
    Overlapping variant regions from other studies: 251 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):237,424,717-237,459,239Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6703639Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2236,516,074236,550,596
    nsv6703639RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2237,424,717237,459,239

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18461630deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18461630Submitted genomicNC_000002.12:g.236
    516074_236550596de
    l
    GRCh38 (hg38)NC_000002.12Chr2236,516,074236,550,596
    nssv18461630RemappedPerfectNC_000002.11:g.237
    424717_237459239de
    l
    GRCh37.p13First PassNC_000002.11Chr2237,424,717237,459,239

    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)
    nssv184616307e-062276262
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