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nsv7038094

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,732,721

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8592 SVs from 125 studies. See in: genome view    
    Submitted genomic106,480,616-110,213,336Question Mark
    Overlapping variant regions from other studies: 8591 SVs from 125 studies. See in: genome view    
    Remapped(Score: Good):107,097,072-110,970,913Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7038094Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2106,480,616110,213,336
    nsv7038094RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2107,097,072110,970,913

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767470inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767470Submitted genomicNC_000002.12:g.106
    480616_110213336in
    v
    GRCh38 (hg38)NC_000002.12Chr2106,480,616110,213,336
    nssv18767470RemappedGoodNC_000002.11:g.107
    097072_110970913in
    v
    GRCh37.p13First PassNC_000002.11Chr2107,097,072110,970,913

    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)
    nssv187674702.9e-058273862
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