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nsv7047201

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,059,340

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2687 SVs from 91 studies. See in: genome view    
    Submitted genomic113,135,467-114,194,806Question Mark
    Overlapping variant regions from other studies: 2695 SVs from 91 studies. See in: genome view    
    Remapped(Score: Perfect):113,893,044-114,952,383Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7047201Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2113,135,467114,194,806
    nsv7047201RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2113,893,044114,952,383

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767545inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767545Submitted genomicNC_000002.12:g.113
    135467_114194806in
    v
    GRCh38 (hg38)NC_000002.12Chr2113,135,467114,194,806
    nssv18767545RemappedPerfectNC_000002.11:g.113
    893044_114952383in
    v
    GRCh37.p13First PassNC_000002.11Chr2113,893,044114,952,383

    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)
    nssv187675454e-061276260
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