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nsv6934352

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:31

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 105 SVs from 24 studies. See in: genome view    
    Submitted genomic125,051,922-125,051,952Question Mark
    Overlapping variant regions from other studies: 105 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):125,536,468-125,536,498Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6934352Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12125,051,922125,051,952
    nsv6934352RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12125,536,468125,536,498

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18355937deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18355937Submitted genomicNC_000012.12:g.125
    051922_125051952de
    l
    GRCh38 (hg38)NC_000012.12Chr12125,051,922125,051,952
    nssv18355937RemappedPerfectNC_000012.11:g.125
    536468_125536498de
    l
    GRCh37.p13First PassNC_000012.11Chr12125,536,468125,536,498

    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)
    nssv183559370.002335220476
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