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nsv6781526

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,342

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 102 SVs from 23 studies. See in: genome view    
    Submitted genomic148,458,876-148,474,217Question Mark
    Overlapping variant regions from other studies: 102 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):147,838,439-147,853,780Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6781526Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5148,458,876148,474,217
    nsv6781526RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5147,838,439147,853,780

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18508464deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18508464Submitted genomicNC_000005.10:g.148
    458876_148474217de
    l
    GRCh38 (hg38)NC_000005.10Chr5148,458,876148,474,217
    nssv18508464RemappedPerfectNC_000005.9:g.1478
    38439_147853780del
    GRCh37.p13First PassNC_000005.9Chr5147,838,439147,853,780

    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)
    nssv185084644e-061275306
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