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nsv7003776

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:98,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 561 SVs from 54 studies. See in: genome view    
    Submitted genomic77,971,501-78,069,800Question Mark
    Overlapping variant regions from other studies: 539 SVs from 55 studies. See in: genome view    
    Remapped(Score: Pass):75,683,457-75,829,800Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7003776Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1877,971,50178,069,800
    nsv7003776RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1875,683,45775,829,800

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18635356duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18635356Submitted genomicNC_000018.10:g.779
    71501_78069800dup
    GRCh38 (hg38)NC_000018.10Chr1877,971,50178,069,800
    nssv18635356RemappedPassNC_000018.9:g.7568
    3457_75829800dup
    GRCh37.p13First PassNC_000018.9Chr1875,683,45775,829,800

    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)
    nssv186353567e-062275858
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