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nsv6966467

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:456

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 83 SVs from 19 studies. See in: genome view    
    Submitted genomic96,212,732-96,213,187Question Mark
    Overlapping variant regions from other studies: 83 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):96,679,069-96,679,524Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6966467Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1496,212,73296,213,187
    nsv6966467RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1496,679,06996,679,524

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18616249duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18616249Submitted genomicNC_000014.9:g.9621
    2732_96213187dup
    GRCh38 (hg38)NC_000014.9Chr1496,212,73296,213,187
    nssv18616249RemappedPerfectNC_000014.8:g.9667
    9069_96679524dup
    GRCh37.p13First PassNC_000014.8Chr1496,679,06996,679,524

    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)
    nssv18616249<0.00143242470
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