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nsv7010192

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,346

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 128 SVs from 37 studies. See in: genome view    
    Submitted genomic53,900,519-53,912,864Question Mark
    Overlapping variant regions from other studies: 128 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):54,403,773-54,416,118Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7010192Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1953,900,51953,912,864
    nsv7010192RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1954,403,77354,416,118

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18639500duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18639500Submitted genomicNC_000019.10:g.539
    00519_53912864dup
    GRCh38 (hg38)NC_000019.10Chr1953,900,51953,912,864
    nssv18639500RemappedPerfectNC_000019.9:g.5440
    3773_54416118dup
    GRCh37.p13First PassNC_000019.9Chr1954,403,77354,416,118

    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)
    nssv186395004e-061275506
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