U.S. flag

An official website of the United States government

nsv6489865

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,594

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 117 SVs from 23 studies. See in: genome view    
    Submitted genomic125,955,841-125,972,434Question Mark
    Overlapping variant regions from other studies: 117 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):126,440,387-126,456,980Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6489865Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12125,955,841125,972,434
    nsv6489865RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12126,440,387126,456,980

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18193717duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18193717Submitted genomicNC_000012.12:g.125
    955841_125972434du
    p
    GRCh38 (hg38)NC_000012.12Chr12125,955,841125,972,434
    nssv18193717RemappedPerfectNC_000012.11:g.126
    440387_126456980du
    p
    GRCh37.p13First PassNC_000012.11Chr12126,440,387126,456,980

    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)
    nssv18193717<0.001139304
    Support Center