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nsv6752520

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,304

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 220 SVs from 46 studies. See in: genome view    
    Submitted genomic68,053,576-68,066,879Question Mark
    Overlapping variant regions from other studies: 220 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):68,919,294-68,932,597Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6752520Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr468,053,57668,066,879
    nsv6752520RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr468,919,29468,932,597

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18500637deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18500637Submitted genomicNC_000004.12:g.680
    53576_68066879del
    GRCh38 (hg38)NC_000004.12Chr468,053,57668,066,879
    nssv18500637RemappedPerfectNC_000004.11:g.689
    19294_68932597del
    GRCh37.p13First PassNC_000004.11Chr468,919,29468,932,597

    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)
    nssv185006377e-062276248
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