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nsv6711235

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:46,150

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 126 SVs from 29 studies. See in: genome view    
    Submitted genomic16,439,049-16,485,198Question Mark
    Overlapping variant regions from other studies: 126 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):16,480,556-16,526,705Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6711235Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr316,439,04916,485,198
    nsv6711235RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr316,480,55616,526,705

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18475990deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18475990Submitted genomicNC_000003.12:g.164
    39049_16485198del
    GRCh38 (hg38)NC_000003.12Chr316,439,04916,485,198
    nssv18475990RemappedPerfectNC_000003.11:g.164
    80556_16526705del
    GRCh37.p13First PassNC_000003.11Chr316,480,55616,526,705

    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)
    nssv184759904e-061276230
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