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nsv6877430

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 235 SVs from 23 studies. See in: genome view    
    Submitted genomic14,302,201-14,304,200Question Mark
    Overlapping variant regions from other studies: 241 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):14,302,200-14,304,199Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6877430Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr914,302,20114,304,200
    nsv6877430RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr914,302,20014,304,199

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18746179duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18746179Submitted genomicNC_000009.12:g.143
    02201_14304200dup
    GRCh38 (hg38)NC_000009.12Chr914,302,20114,304,200
    nssv18746179RemappedPerfectNC_000009.11:g.143
    02200_14304199dup
    GRCh37.p13First PassNC_000009.11Chr914,302,20014,304,199

    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)
    nssv187461797e-062272012
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