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nsv6793015

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:117,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 687 SVs from 75 studies. See in: genome view    
    Submitted genomic179,523,101-179,640,200Question Mark
    Overlapping variant regions from other studies: 687 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):178,950,102-179,067,201Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6793015Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5179,523,101179,640,200
    nsv6793015RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5178,950,102179,067,201

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18700026duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18700026Submitted genomicNC_000005.10:g.179
    523101_179640200du
    p
    GRCh38 (hg38)NC_000005.10Chr5179,523,101179,640,200
    nssv18700026RemappedPerfectNC_000005.9:g.1789
    50102_179067201dup
    GRCh37.p13First PassNC_000005.9Chr5178,950,102179,067,201

    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)
    nssv187000260.0091752204848
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