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nsv6693272

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:675

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 81 SVs from 19 studies. See in: genome view    
    Submitted genomic228,076,341-228,077,015Question Mark
    Overlapping variant regions from other studies: 81 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):228,941,057-228,941,731Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6693272Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2228,076,341228,077,015
    nsv6693272RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2228,941,057228,941,731

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18450196deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18450196Submitted genomicNC_000002.12:g.228
    076341_228077015de
    l
    GRCh38 (hg38)NC_000002.12Chr2228,076,341228,077,015
    nssv18450196RemappedPerfectNC_000002.11:g.228
    941057_228941731de
    l
    GRCh37.p13First PassNC_000002.11Chr2228,941,057228,941,731

    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)
    nssv184501967e-062273728
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