U.S. flag

An official website of the United States government

nsv6899262

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 134 SVs from 42 studies. See in: genome view    
    Submitted genomic3,396,601-3,399,200Question Mark
    Overlapping variant regions from other studies: 134 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):3,417,831-3,420,430Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6899262Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr113,396,6013,399,200
    nsv6899262RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr113,417,8313,420,430

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18349070deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18349070Submitted genomicNC_000011.10:g.339
    6601_3399200del
    GRCh38 (hg38)NC_000011.10Chr113,396,6013,399,200
    nssv18349070RemappedPerfectNC_000011.9:g.3417
    831_3420430del
    GRCh37.p13First PassNC_000011.9Chr113,417,8313,420,430

    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)
    nssv183490700.0153948273590
    Support Center