U.S. flag

An official website of the United States government

nsv6993667

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,464,263

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 9276 SVs from 111 studies. See in: genome view    
    Submitted genomic78,709,580-81,173,842Question Mark
    Overlapping variant regions from other studies: 9029 SVs from 111 studies. See in: genome view    
    Remapped(Score: Good):76,705,662-79,147,642Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6993667Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1778,709,58081,173,842
    nsv6993667RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1776,705,66279,147,642

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18413426deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18413426Submitted genomicNC_000017.11:g.787
    09580_81173842del
    GRCh38 (hg38)NC_000017.11Chr1778,709,58081,173,842
    nssv18413426RemappedGoodNC_000017.10:g.767
    05662_79147642del
    GRCh37.p13First PassNC_000017.10Chr1776,705,66279,147,642

    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)
    nssv184134264e-061275778
    Support Center