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nsv6936840

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,792

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 96 SVs from 29 studies. See in: genome view    
    Submitted genomic120,005,657-120,008,448Question Mark
    Overlapping variant regions from other studies: 96 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):120,443,461-120,446,252Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6936840Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12120,005,657120,008,448
    nsv6936840RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12120,443,461120,446,252

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18357048deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18357048Submitted genomicNC_000012.12:g.120
    005657_120008448de
    l
    GRCh38 (hg38)NC_000012.12Chr12120,005,657120,008,448
    nssv18357048RemappedPerfectNC_000012.11:g.120
    443461_120446252de
    l
    GRCh37.p13First PassNC_000012.11Chr12120,443,461120,446,252

    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)
    nssv18357048<0.00128274916
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