U.S. flag

An official website of the United States government

nsv6815891

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:110

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 91 SVs from 21 studies. See in: genome view    
    Submitted genomic150,673,230-150,673,339Question Mark
    Overlapping variant regions from other studies: 91 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):150,994,366-150,994,475Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6815891Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6150,673,230150,673,339
    nsv6815891RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6150,994,366150,994,475

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18711509duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18711509Submitted genomicNC_000006.12:g.150
    673230_150673339du
    p
    GRCh38 (hg38)NC_000006.12Chr6150,673,230150,673,339
    nssv18711509RemappedPerfectNC_000006.11:g.150
    994366_150994475du
    p
    GRCh37.p13First PassNC_000006.11Chr6150,994,366150,994,475

    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)
    nssv187115094e-061227548
    Support Center