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nsv6582461

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,413

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 100 SVs from 28 studies. See in: genome view    
    Submitted genomic112,485,767-112,487,179Question Mark
    Overlapping variant regions from other studies: 100 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):112,923,571-112,924,983Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6582461Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12112,485,767112,487,179
    nsv6582461RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12112,923,571112,924,983

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18222426inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18222426Submitted genomicNC_000012.12:g.112
    485767_112487179in
    v
    GRCh38 (hg38)NC_000012.12Chr12112,485,767112,487,179
    nssv18222426RemappedPerfectNC_000012.11:g.112
    923571_112924983in
    v
    GRCh37.p13First PassNC_000012.11Chr12112,923,571112,924,983

    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)
    nssv18222426<0.001135592
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