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nsv6877895

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,585

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 275 SVs from 29 studies. See in: genome view    
    Submitted genomic14,184,294-14,193,878Question Mark
    Overlapping variant regions from other studies: 280 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):14,184,293-14,193,877Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6877895Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr914,184,29414,193,878
    nsv6877895RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr914,184,29314,193,877

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18732631duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18732631Submitted genomicNC_000009.12:g.141
    84294_14193878dup
    GRCh38 (hg38)NC_000009.12Chr914,184,29414,193,878
    nssv18732631RemappedPerfectNC_000009.11:g.141
    84293_14193877dup
    GRCh37.p13First PassNC_000009.11Chr914,184,29314,193,877

    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)
    nssv187326314e-061274970
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