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nsv6689136

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,986

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 86 SVs from 19 studies. See in: genome view    
    Submitted genomic230,927,846-230,931,831Question Mark
    Overlapping variant regions from other studies: 86 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):231,792,561-231,796,546Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6689136Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2230,927,846230,931,831
    nsv6689136RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2231,792,561231,796,546

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18450822deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18450822Submitted genomicNC_000002.12:g.230
    927846_230931831de
    l
    GRCh38 (hg38)NC_000002.12Chr2230,927,846230,931,831
    nssv18450822RemappedPerfectNC_000002.11:g.231
    792561_231796546de
    l
    GRCh37.p13First PassNC_000002.11Chr2231,792,561231,796,546

    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)
    nssv184508224e-061276134
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