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nsv6929226

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:22,547

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 122 SVs from 33 studies. See in: genome view    
    Submitted genomic120,037,247-120,059,793Question Mark
    Overlapping variant regions from other studies: 122 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):120,475,051-120,497,597Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6929226Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12120,037,247120,059,793
    nsv6929226RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12120,475,051120,497,597

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18593073duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18593073Submitted genomicNC_000012.12:g.120
    037247_120059793du
    p
    GRCh38 (hg38)NC_000012.12Chr12120,037,247120,059,793
    nssv18593073RemappedPerfectNC_000012.11:g.120
    475051_120497597du
    p
    GRCh37.p13First PassNC_000012.11Chr12120,475,051120,497,597

    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)
    nssv185930734e-061276094
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