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nsv6795323

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,556

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 95 SVs from 21 studies. See in: genome view    
    Submitted genomic148,463,026-148,466,581Question Mark
    Overlapping variant regions from other studies: 95 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):147,842,589-147,846,144Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6795323Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5148,463,026148,466,581
    nsv6795323RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5147,842,589147,846,144

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18506447deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18506447Submitted genomicNC_000005.10:g.148
    463026_148466581de
    l
    GRCh38 (hg38)NC_000005.10Chr5148,463,026148,466,581
    nssv18506447RemappedPerfectNC_000005.9:g.1478
    42589_147846144del
    GRCh37.p13First PassNC_000005.9Chr5147,842,589147,846,144

    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)
    nssv18506447<0.001126274356
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