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nsv6944211

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 55 SVs from 16 studies. See in: genome view    
    Submitted genomic24,331,001-24,335,500Question Mark
    Overlapping variant regions from other studies: 57 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):24,800,207-24,804,706Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6944211Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1424,331,00124,335,500
    nsv6944211RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1424,800,20724,804,706

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18611846duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18611846Submitted genomicNC_000014.9:g.2433
    1001_24335500dup
    GRCh38 (hg38)NC_000014.9Chr1424,331,00124,335,500
    nssv18611846RemappedPerfectNC_000014.8:g.2480
    0207_24804706dup
    GRCh37.p13First PassNC_000014.8Chr1424,800,20724,804,706

    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)
    nssv186118464e-061272926
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