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nsv6936441

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:98

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 91 SVs from 25 studies. See in: genome view    
    Submitted genomic43,995,200-43,995,297Question Mark
    Overlapping variant regions from other studies: 91 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):44,389,003-44,389,100Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6936441Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1243,995,20043,995,297
    nsv6936441RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1244,389,00344,389,100

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18596518duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18596518Submitted genomicNC_000012.12:g.439
    95200_43995297dup
    GRCh38 (hg38)NC_000012.12Chr1243,995,20043,995,297
    nssv18596518RemappedPerfectNC_000012.11:g.443
    89003_44389100dup
    GRCh37.p13First PassNC_000012.11Chr1244,389,00344,389,100

    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)
    nssv185965182.6e-056223928
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