U.S. flag

An official website of the United States government

nsv6926199

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,190

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 100 SVs from 25 studies. See in: genome view    
    Submitted genomic29,820,517-29,825,706Question Mark
    Overlapping variant regions from other studies: 100 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):30,394,654-30,399,843Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6926199Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1329,820,51729,825,706
    nsv6926199RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1330,394,65430,399,843

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18377044deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18377044Submitted genomicNC_000013.11:g.298
    20517_29825706del
    GRCh38 (hg38)NC_000013.11Chr1329,820,51729,825,706
    nssv18377044RemappedPerfectNC_000013.10:g.303
    94654_30399843del
    GRCh37.p13First PassNC_000013.10Chr1330,394,65430,399,843

    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)
    nssv183770444e-061276234
    Support Center