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nsv7040291

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:637,678

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1646 SVs from 81 studies. See in: genome view    
    Submitted genomic127,202,908-127,840,585Question Mark
    Overlapping variant regions from other studies: 1646 SVs from 81 studies. See in: genome view    
    Remapped(Score: Perfect):127,960,484-128,598,159Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7040291Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2127,202,908127,840,585
    nsv7040291RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2127,960,484128,598,159

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765309inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765309Submitted genomicNC_000002.12:g.127
    202908_127840585in
    v
    GRCh38 (hg38)NC_000002.12Chr2127,202,908127,840,585
    nssv18765309RemappedPerfectNC_000002.11:g.127
    960484_128598159in
    v
    GRCh37.p13First PassNC_000002.11Chr2127,960,484128,598,159

    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)
    nssv18765309<0.001102274362
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