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nsv6966835

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:335

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 74 SVs from 15 studies. See in: genome view    
    Submitted genomic64,937,744-64,938,078Question Mark
    Overlapping variant regions from other studies: 74 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):65,404,462-65,404,796Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6966835Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1464,937,74464,938,078
    nsv6966835RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1465,404,46265,404,796

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18614590duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18614590Submitted genomicNC_000014.9:g.6493
    7744_64938078dup
    GRCh38 (hg38)NC_000014.9Chr1464,937,74464,938,078
    nssv18614590RemappedPerfectNC_000014.8:g.6540
    4462_65404796dup
    GRCh37.p13First PassNC_000014.8Chr1465,404,46265,404,796

    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)
    nssv186145908e-062233196
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