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nsv7010429

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:359

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 86 SVs from 18 studies. See in: genome view    
    Submitted genomic10,767,981-10,768,339Question Mark
    Overlapping variant regions from other studies: 86 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):10,878,657-10,879,015Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7010429Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1910,767,98110,768,339
    nsv7010429RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1910,878,65710,879,015

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18638492duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18638492Submitted genomicNC_000019.10:g.107
    67981_10768339dup
    GRCh38 (hg38)NC_000019.10Chr1910,767,98110,768,339
    nssv18638492RemappedPerfectNC_000019.9:g.1087
    8657_10879015dup
    GRCh37.p13First PassNC_000019.9Chr1910,878,65710,879,015

    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)
    nssv186384924e-061243462
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