nsv6978217

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:701,829

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2677 SVs from 94 studies. See in: genome view    
    Submitted genomic2,107,110-2,808,938Question Mark
    Overlapping variant regions from other studies: 2677 SVs from 94 studies. See in: genome view    
    Remapped(Score: Perfect):2,010,404-2,712,232Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6978217Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr172,107,1102,808,938
    nsv6978217RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr172,010,4042,712,232

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18625718duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18625718Submitted genomicNC_000017.11:g.210
    7110_2808938dup
    GRCh38 (hg38)NC_000017.11Chr172,107,1102,808,938
    nssv18625718RemappedPerfectNC_000017.10:g.201
    0404_2712232dup
    GRCh37.p13First PassNC_000017.10Chr172,010,4042,712,232

    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)
    nssv186257184e-061275104
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