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nsv6785893

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:72,905

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 191 SVs from 35 studies. See in: genome view    
    Submitted genomic172,370,526-172,443,430Question Mark
    Overlapping variant regions from other studies: 191 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):171,797,530-171,870,434Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6785893Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5172,370,526172,443,430
    nsv6785893RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5171,797,530171,870,434

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18702358duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18702358Submitted genomicNC_000005.10:g.172
    370526_172443430du
    p
    GRCh38 (hg38)NC_000005.10Chr5172,370,526172,443,430
    nssv18702358RemappedPerfectNC_000005.9:g.1717
    97530_171870434dup
    GRCh37.p13First PassNC_000005.9Chr5171,797,530171,870,434

    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)
    nssv187023587e-062275288
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