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nsv6828041

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:32,968

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 155 SVs from 37 studies. See in: genome view    
    Submitted genomic39,718,782-39,751,749Question Mark
    Overlapping variant regions from other studies: 155 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):39,758,381-39,791,348Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6828041Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr739,718,78239,751,749
    nsv6828041RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr739,758,38139,791,348

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18726375duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18726375Submitted genomicNC_000007.14:g.397
    18782_39751749dup
    GRCh38 (hg38)NC_000007.14Chr739,718,78239,751,749
    nssv18726375RemappedPerfectNC_000007.13:g.397
    58381_39791348dup
    GRCh37.p13First PassNC_000007.13Chr739,758,38139,791,348

    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)
    nssv187263757e-062275408
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