U.S. flag

An official website of the United States government

nsv6876968

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,663

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 187 SVs from 30 studies. See in: genome view    
    Submitted genomic26,941,354-26,947,016Question Mark
    Overlapping variant regions from other studies: 193 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):26,941,352-26,947,014Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6876968Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr926,941,35426,947,016
    nsv6876968RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr926,941,35226,947,014

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18566741deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18566741Submitted genomicNC_000009.12:g.269
    41354_26947016del
    GRCh38 (hg38)NC_000009.12Chr926,941,35426,947,016
    nssv18566741RemappedPerfectNC_000009.11:g.269
    41352_26947014del
    GRCh37.p13First PassNC_000009.11Chr926,941,35226,947,014

    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)
    nssv185667414e-061276242
    Support Center