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nsv7002151

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,379,975

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6778 SVs from 110 studies. See in: genome view    
    Submitted genomic58,224,549-60,604,523Question Mark
    Overlapping variant regions from other studies: 6779 SVs from 110 studies. See in: genome view    
    Remapped(Score: Perfect):55,891,781-58,271,756Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7002151Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1858,224,54960,604,523
    nsv7002151RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1855,891,78158,271,756

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18634543duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18634543Submitted genomicNC_000018.10:g.582
    24549_60604523dup
    GRCh38 (hg38)NC_000018.10Chr1858,224,54960,604,523
    nssv18634543RemappedPerfectNC_000018.9:g.5589
    1781_58271756dup
    GRCh37.p13First PassNC_000018.9Chr1855,891,78158,271,756

    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)
    nssv186345434e-061274444
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