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nsv7073953

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:563,153

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2476 SVs from 90 studies. See in: genome view    
    Submitted genomic84,385,564-84,948,716Question Mark
    Overlapping variant regions from other studies: 2476 SVs from 90 studies. See in: genome view    
    Remapped(Score: Perfect):84,419,170-84,982,322Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073953Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1684,385,56484,948,716
    nsv7073953RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1684,419,17084,982,322

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756650inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756650Submitted genomicNC_000016.10:g.843
    85564_84948716inv
    GRCh38 (hg38)NC_000016.10Chr1684,385,56484,948,716
    nssv18756650RemappedPerfectNC_000016.9:g.8441
    9170_84982322inv
    GRCh37.p13First PassNC_000016.9Chr1684,419,17084,982,322

    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)
    nssv187566503.6e-0510274120
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