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nsv6791832

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,749

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 34 studies. See in: genome view    
    Submitted genomic24,295,149-24,312,897Question Mark
    Overlapping variant regions from other studies: 111 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):24,295,377-24,313,125Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6791832Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr624,295,14924,312,897
    nsv6791832RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr624,295,37724,313,125

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18711161duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18711161Submitted genomicNC_000006.12:g.242
    95149_24312897dup
    GRCh38 (hg38)NC_000006.12Chr624,295,14924,312,897
    nssv18711161RemappedPerfectNC_000006.11:g.242
    95377_24313125dup
    GRCh37.p13First PassNC_000006.11Chr624,295,37724,313,125

    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)
    nssv187111611.4e-054276088
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