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nsv6461901

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:28,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 132 SVs from 29 studies. See in: genome view    
    Submitted genomic107,755,001-107,783,900Question Mark
    Overlapping variant regions from other studies: 132 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):108,148,778-108,177,677Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6461901Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12107,755,001107,783,900
    nsv6461901RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12108,148,778108,177,677

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18196253duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18196253Submitted genomicNC_000012.12:g.107
    755001_107783900du
    p
    GRCh38 (hg38)NC_000012.12Chr12107,755,001107,783,900
    nssv18196253RemappedPerfectNC_000012.11:g.108
    148778_108177677du
    p
    GRCh37.p13First PassNC_000012.11Chr12108,148,778108,177,677

    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)
    nssv18196253<0.0011639238
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