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nsv7048071

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,501

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 136 SVs from 31 studies. See in: genome view    
    Submitted genomic132,735,909-132,740,409Question Mark
    Overlapping variant regions from other studies: 136 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):133,493,482-133,497,982Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048071Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2132,735,909132,740,409
    nsv7048071RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2133,493,482133,497,982

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765731inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765731Submitted genomicNC_000002.12:g.132
    735909_132740409in
    v
    GRCh38 (hg38)NC_000002.12Chr2132,735,909132,740,409
    nssv18765731RemappedPerfectNC_000002.11:g.133
    493482_133497982in
    v
    GRCh37.p13First PassNC_000002.11Chr2133,493,482133,497,982

    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)
    nssv187657311.1e-053276252
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