U.S. flag

An official website of the United States government

nsv6776822

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:40,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 275 SVs from 45 studies. See in: genome view    
    Submitted genomic79,243,301-79,283,300Question Mark
    Overlapping variant regions from other studies: 275 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):78,539,124-78,579,123Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6776822Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr579,243,30179,283,300
    nsv6776822RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr578,539,12478,579,123

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18707575duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18707575Submitted genomicNC_000005.10:g.792
    43301_79283300dup
    GRCh38 (hg38)NC_000005.10Chr579,243,30179,283,300
    nssv18707575RemappedPerfectNC_000005.9:g.7853
    9124_78579123dup
    GRCh37.p13First PassNC_000005.9Chr578,539,12478,579,123

    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)
    nssv187075754e-061274704
    Support Center