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nsv6932826

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:216

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 163 SVs from 49 studies. See in: genome view    
    Submitted genomic127,018,092-127,018,307Question Mark
    Overlapping variant regions from other studies: 163 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):127,502,637-127,502,852Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6932826Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12127,018,092127,018,307
    nsv6932826RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12127,502,637127,502,852

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18357318deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18357318Submitted genomicNC_000012.12:g.127
    018092_127018307de
    l
    GRCh38 (hg38)NC_000012.12Chr12127,018,092127,018,307
    nssv18357318RemappedPerfectNC_000012.11:g.127
    502637_127502852de
    l
    GRCh37.p13First PassNC_000012.11Chr12127,502,637127,502,852

    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)
    nssv183573180.595143967242110
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