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nsv7012699

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:62,019

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 436 SVs from 40 studies. See in: genome view    
    Submitted genomic63,415,955-63,477,973Question Mark
    Overlapping variant regions from other studies: 436 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):61,083,188-61,145,206Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7012699Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1863,415,95563,477,973
    nsv7012699RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1861,083,18861,145,206

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18633635duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18633635Submitted genomicNC_000018.10:g.634
    15955_63477973dup
    GRCh38 (hg38)NC_000018.10Chr1863,415,95563,477,973
    nssv18633635RemappedPerfectNC_000018.9:g.6108
    3188_61145206dup
    GRCh37.p13First PassNC_000018.9Chr1861,083,18861,145,206

    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)
    nssv186336354e-061274418
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