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nsv6757071

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,131

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 190 SVs from 42 studies. See in: genome view    
    Submitted genomic68,068,626-68,070,756Question Mark
    Overlapping variant regions from other studies: 190 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):68,934,344-68,936,474Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6757071Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr468,068,62668,070,756
    nsv6757071RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr468,934,34468,936,474

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18500639deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18500639Submitted genomicNC_000004.12:g.680
    68626_68070756del
    GRCh38 (hg38)NC_000004.12Chr468,068,62668,070,756
    nssv18500639RemappedPerfectNC_000004.11:g.689
    34344_68936474del
    GRCh37.p13First PassNC_000004.11Chr468,934,34468,936,474

    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)
    nssv185006394e-061275916
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