U.S. flag

An official website of the United States government

nsv6977592

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,347

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 208 SVs from 38 studies. See in: genome view    
    Submitted genomic3,246,328-3,262,674Question Mark
    Overlapping variant regions from other studies: 208 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):3,296,328-3,312,674Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6977592Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr163,246,3283,262,674
    nsv6977592RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr163,296,3283,312,674

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18400563deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18400563Submitted genomicNC_000016.10:g.324
    6328_3262674del
    GRCh38 (hg38)NC_000016.10Chr163,246,3283,262,674
    nssv18400563RemappedPerfectNC_000016.9:g.3296
    328_3312674del
    GRCh37.p13First PassNC_000016.9Chr163,296,3283,312,674

    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)
    nssv184005634e-061275984
    Support Center