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nsv6788181

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:382

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 72 SVs from 11 studies. See in: genome view    
    Submitted genomic148,451,339-148,451,720Question Mark
    Overlapping variant regions from other studies: 72 SVs from 11 studies. See in: genome view    
    Remapped(Score: Perfect):147,830,902-147,831,283Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6788181Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5148,451,339148,451,720
    nsv6788181RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5147,830,902147,831,283

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18700505duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18700505Submitted genomicNC_000005.10:g.148
    451339_148451720du
    p
    GRCh38 (hg38)NC_000005.10Chr5148,451,339148,451,720
    nssv18700505RemappedPerfectNC_000005.9:g.1478
    30902_147831283dup
    GRCh37.p13First PassNC_000005.9Chr5147,830,902147,831,283

    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)
    nssv187005054e-061241338
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