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nsv6367961

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:670

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 101 SVs from 21 studies. See in: genome view    
    Submitted genomic171,856,041-171,856,710Question Mark
    Overlapping variant regions from other studies: 101 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):171,573,831-171,574,500Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6367961Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3171,856,041171,856,710
    nsv6367961RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3171,573,831171,574,500

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18098724deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18098724Submitted genomicNC_000003.12:g.171
    856041_171856710de
    l
    GRCh38 (hg38)NC_000003.12Chr3171,856,041171,856,710
    nssv18098724RemappedPerfectNC_000003.11:g.171
    573831_171574500de
    l
    GRCh37.p13First PassNC_000003.11Chr3171,573,831171,574,500

    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)
    nssv18098724<0.001838410
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