U.S. flag

An official website of the United States government

nsv6784012

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:919,309

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2454 SVs from 92 studies. See in: genome view    
    Submitted genomic9,546,200-10,465,508Question Mark
    Overlapping variant regions from other studies: 2454 SVs from 92 studies. See in: genome view    
    Remapped(Score: Perfect):9,546,433-10,465,741Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6784012Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr69,546,20010,465,508
    nsv6784012RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr69,546,43310,465,741

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18531816deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18531816Submitted genomicNC_000006.12:g.954
    6200_10465508del
    GRCh38 (hg38)NC_000006.12Chr69,546,20010,465,508
    nssv18531816RemappedPerfectNC_000006.11:g.954
    6433_10465741del
    GRCh37.p13First PassNC_000006.11Chr69,546,43310,465,741

    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)
    nssv185318164e-061276212
    Support Center