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nsv7026127

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:294

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 663 SVs from 48 studies. See in: genome view    
    Submitted genomic20,242,538-20,242,831Question Mark
    Overlapping variant regions from other studies: 647 SVs from 48 studies. See in: genome view    
    Remapped(Score: Perfect):20,230,061-20,230,354Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7026127Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2220,242,53820,242,831
    nsv7026127RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2220,230,06120,230,354

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18651753duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18651753Submitted genomicNC_000022.11:g.202
    42538_20242831dup
    GRCh38 (hg38)NC_000022.11Chr2220,242,53820,242,831
    nssv18651753RemappedPerfectNC_000022.10:g.202
    30061_20230354dup
    GRCh37.p13First PassNC_000022.10Chr2220,230,06120,230,354

    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)
    nssv18651753<0.00141229578
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