U.S. flag

An official website of the United States government

nsv6944386

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:95

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 124 SVs from 20 studies. See in: genome view    
    Submitted genomic39,030,893-39,030,987Question Mark
    Overlapping variant regions from other studies: 124 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):39,605,030-39,605,124Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6944386Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1339,030,89339,030,987
    nsv6944386RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1339,605,03039,605,124

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18600950duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18600950Submitted genomicNC_000013.11:g.390
    30893_39030987dup
    GRCh38 (hg38)NC_000013.11Chr1339,030,89339,030,987
    nssv18600950RemappedPerfectNC_000013.10:g.396
    05030_39605124dup
    GRCh37.p13First PassNC_000013.10Chr1339,605,03039,605,124

    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)
    nssv18600950<0.00163222040
    Support Center