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nsv6475929

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,693

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 109 SVs from 30 studies. See in: genome view    
    Submitted genomic111,422,706-111,429,398Question Mark
    Overlapping variant regions from other studies: 109 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):111,860,510-111,867,202Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6475929Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12111,422,706111,429,398
    nsv6475929RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12111,860,510111,867,202

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17996971deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17996971Submitted genomicNC_000012.12:g.111
    422706_111429398de
    l
    GRCh38 (hg38)NC_000012.12Chr12111,422,706111,429,398
    nssv17996971RemappedPerfectNC_000012.11:g.111
    860510_111867202de
    l
    GRCh37.p13First PassNC_000012.11Chr12111,860,510111,867,202

    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)
    nssv17996971<0.0011039274
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