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nsv6748936

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:620

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 196 SVs from 42 studies. See in: genome view    
    Submitted genomic68,092,538-68,093,157Question Mark
    Overlapping variant regions from other studies: 196 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):68,958,256-68,958,875Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6748936Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr468,092,53868,093,157
    nsv6748936RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr468,958,25668,958,875

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18500643deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18500643Submitted genomicNC_000004.12:g.680
    92538_68093157del
    GRCh38 (hg38)NC_000004.12Chr468,092,53868,093,157
    nssv18500643RemappedPerfectNC_000004.11:g.689
    58256_68958875del
    GRCh37.p13First PassNC_000004.11Chr468,958,25668,958,875

    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)
    nssv18500643<0.00198244090
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