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nsv6614143

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:953

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 119 SVs from 21 studies. See in: genome view    
    Submitted genomic110,431,957-110,432,909Question Mark
    Overlapping variant regions from other studies: 119 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):110,753,160-110,754,112Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6614143Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6110,431,957110,432,909
    nsv6614143RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6110,753,160110,754,112

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18136680deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18136680Submitted genomicNC_000006.12:g.110
    431957_110432909de
    l
    GRCh38 (hg38)NC_000006.12Chr6110,431,957110,432,909
    nssv18136680RemappedPerfectNC_000006.11:g.110
    753160_110754112de
    l
    GRCh37.p13First PassNC_000006.11Chr6110,753,160110,754,112

    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)
    nssv18136680<0.001937530
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