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nsv7046677

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:179,359

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 505 SVs from 66 studies. See in: genome view    
    Submitted genomic133,536,266-133,715,624Question Mark
    Overlapping variant regions from other studies: 505 SVs from 66 studies. See in: genome view    
    Remapped(Score: Perfect):134,293,837-134,473,195Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7046677Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2133,536,266133,715,624
    nsv7046677RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2134,293,837134,473,195

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765744inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765744Submitted genomicNC_000002.12:g.133
    536266_133715624in
    v
    GRCh38 (hg38)NC_000002.12Chr2133,536,266133,715,624
    nssv18765744RemappedPerfectNC_000002.11:g.134
    293837_134473195in
    v
    GRCh37.p13First PassNC_000002.11Chr2134,293,837134,473,195

    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)
    nssv187657444e-061276268
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