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nsv6920730

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:23,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 333 SVs from 57 studies. See in: genome view    
    Submitted genomic7,768,101-7,791,400Question Mark
    Overlapping variant regions from other studies: 333 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):7,920,697-7,943,996Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6920730Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr127,768,1017,791,400
    nsv6920730RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr127,920,6977,943,996

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18598606duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18598606Submitted genomicNC_000012.12:g.776
    8101_7791400dup
    GRCh38 (hg38)NC_000012.12Chr127,768,1017,791,400
    nssv18598606RemappedPerfectNC_000012.11:g.792
    0697_7943996dup
    GRCh37.p13First PassNC_000012.11Chr127,920,6977,943,996

    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)
    nssv18598606<0.00144273808
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