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nsv6473973

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:36,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 477 SVs from 68 studies. See in: genome view    
    Submitted genomic8,208,701-8,245,000Question Mark
    Overlapping variant regions from other studies: 477 SVs from 68 studies. See in: genome view    
    Remapped(Score: Perfect):8,361,297-8,397,596Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6473973Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr128,208,7018,245,000
    nsv6473973RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr128,361,2978,397,596

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18177326duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18177326Submitted genomicNC_000012.12:g.820
    8701_8245000dup
    GRCh38 (hg38)NC_000012.12Chr128,208,7018,245,000
    nssv18177326RemappedPerfectNC_000012.11:g.836
    1297_8397596dup
    GRCh37.p13First PassNC_000012.11Chr128,361,2978,397,596

    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)
    nssv181773260.193750038958
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