U.S. flag

An official website of the United States government

nsv6977215

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 171 SVs from 41 studies. See in: genome view    
    Submitted genomic4,083,201-4,091,200Question Mark
    Overlapping variant regions from other studies: 171 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):4,133,202-4,141,201Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6977215Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr164,083,2014,091,200
    nsv6977215RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr164,133,2024,141,201

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18400941deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18400941Submitted genomicNC_000016.10:g.408
    3201_4091200del
    GRCh38 (hg38)NC_000016.10Chr164,083,2014,091,200
    nssv18400941RemappedPerfectNC_000016.9:g.4133
    202_4141201del
    GRCh37.p13First PassNC_000016.9Chr164,133,2024,141,201

    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)
    nssv184009410.004977252156
    Support Center