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nsv6916591

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:42,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 174 SVs from 52 studies. See in: genome view    
    Submitted genomic17,708,484-17,750,483Question Mark
    Overlapping variant regions from other studies: 174 SVs from 52 studies. See in: genome view    
    Remapped(Score: Perfect):17,730,031-17,772,030Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6916591Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1117,708,48417,750,483
    nsv6916591RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1117,730,03117,772,030

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18573858duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18573858Submitted genomicNC_000011.10:g.177
    08484_17750483dup
    GRCh38 (hg38)NC_000011.10Chr1117,708,48417,750,483
    nssv18573858RemappedPerfectNC_000011.9:g.1773
    0031_17772030dup
    GRCh37.p13First PassNC_000011.9Chr1117,730,03117,772,030

    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)
    nssv185738581.1e-053275706
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