U.S. flag

An official website of the United States government

nsv6937858

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 132 SVs from 27 studies. See in: genome view    
    Submitted genomic14,739,201-14,742,300Question Mark
    Overlapping variant regions from other studies: 133 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):14,892,135-14,895,234Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6937858Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1214,739,20114,742,300
    nsv6937858RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1214,892,13514,895,234

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18595694duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18595694Submitted genomicNC_000012.12:g.147
    39201_14742300dup
    GRCh38 (hg38)NC_000012.12Chr1214,739,20114,742,300
    nssv18595694RemappedPerfectNC_000012.11:g.148
    92135_14895234dup
    GRCh37.p13First PassNC_000012.11Chr1214,892,13514,895,234

    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)
    nssv185956944e-061273416
    Support Center