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nsv7004911

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:746,623

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2813 SVs from 85 studies. See in: genome view    
    Submitted genomic16,817,573-17,564,195Question Mark
    Overlapping variant regions from other studies: 2813 SVs from 85 studies. See in: genome view    
    Remapped(Score: Perfect):16,928,384-17,675,004Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7004911Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1916,817,57317,564,195
    nsv7004911RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1916,928,38417,675,004

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18639294duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18639294Submitted genomicNC_000019.10:g.168
    17573_17564195dup
    GRCh38 (hg38)NC_000019.10Chr1916,817,57317,564,195
    nssv18639294RemappedPerfectNC_000019.9:g.1692
    8384_17675004dup
    GRCh37.p13First PassNC_000019.9Chr1916,928,38417,675,004

    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)
    nssv186392944e-061275242
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