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nsv6997553

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,885

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 131 SVs from 15 studies. See in: genome view    
    Submitted genomic76,001,889-76,004,773Question Mark
    Overlapping variant regions from other studies: 131 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):73,997,970-74,000,854Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6997553Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1776,001,88976,004,773
    nsv6997553RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1773,997,97074,000,854

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18631344duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18631344Submitted genomicNC_000017.11:g.760
    01889_76004773dup
    GRCh38 (hg38)NC_000017.11Chr1776,001,88976,004,773
    nssv18631344RemappedPerfectNC_000017.10:g.739
    97970_74000854dup
    GRCh37.p13First PassNC_000017.10Chr1773,997,97074,000,854

    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)
    nssv186313444e-061273886
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