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nsv6791013

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,587

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 58 SVs from 12 studies. See in: genome view    
    Submitted genomic171,817,550-171,823,136Question Mark
    Overlapping variant regions from other studies: 58 SVs from 12 studies. See in: genome view    
    Remapped(Score: Perfect):171,244,554-171,250,140Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6791013Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5171,817,550171,823,136
    nsv6791013RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5171,244,554171,250,140

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18701715duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18701715Submitted genomicNC_000005.10:g.171
    817550_171823136du
    p
    GRCh38 (hg38)NC_000005.10Chr5171,817,550171,823,136
    nssv18701715RemappedPerfectNC_000005.9:g.1712
    44554_171250140dup
    GRCh37.p13First PassNC_000005.9Chr5171,244,554171,250,140

    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)
    nssv187017154e-061274462
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