U.S. flag

An official website of the United States government

nsv6492805

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:358,271

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1566 SVs from 92 studies. See in: genome view    
    Submitted genomic126,389,353-126,747,623Question Mark
    Overlapping variant regions from other studies: 1566 SVs from 92 studies. See in: genome view    
    Remapped(Score: Perfect):126,873,899-127,232,169Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6492805Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12126,389,353126,747,623
    nsv6492805RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12126,873,899127,232,169

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18186076duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18186076Submitted genomicNC_000012.12:g.126
    389353_126747623du
    p
    GRCh38 (hg38)NC_000012.12Chr12126,389,353126,747,623
    nssv18186076RemappedPerfectNC_000012.11:g.126
    873899_127232169du
    p
    GRCh37.p13First PassNC_000012.11Chr12126,873,899127,232,169

    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)
    nssv18186076<0.0011439300
    Support Center