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nsv7036611

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:752

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 175 SVs from 26 studies. See in: genome view    
    Submitted genomic39,598,794-39,599,545Question Mark
    Overlapping variant regions from other studies: 176 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):40,970,721-40,971,472Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7036611Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2139,598,79439,599,545
    nsv7036611RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2140,970,72140,971,472

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18643979duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18643979Submitted genomicNC_000021.9:g.3959
    8794_39599545dup
    GRCh38 (hg38)NC_000021.9Chr2139,598,79439,599,545
    nssv18643979RemappedPerfectNC_000021.8:g.4097
    0721_40971472dup
    GRCh37.p13First PassNC_000021.8Chr2140,970,72140,971,472

    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)
    nssv186439798.8e-0522256810
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