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nsv6340902

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:774

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 140 SVs from 27 studies. See in: genome view    
    Submitted genomic157,321,055-157,321,828Question Mark
    Overlapping variant regions from other studies: 140 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):158,177,567-158,178,340Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6340902Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2157,321,055157,321,828
    nsv6340902RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2158,177,567158,178,340

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18079791deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18079791Submitted genomicNC_000002.12:g.157
    321055_157321828de
    l
    GRCh38 (hg38)NC_000002.12Chr2157,321,055157,321,828
    nssv18079791RemappedPerfectNC_000002.11:g.158
    177567_158178340de
    l
    GRCh37.p13First PassNC_000002.11Chr2158,177,567158,178,340

    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)
    nssv18079791<0.001438564
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