U.S. flag

An official website of the United States government

nsv6916016

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:444

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 79 SVs from 19 studies. See in: genome view    
    Submitted genomic74,170,227-74,170,670Question Mark
    Overlapping variant regions from other studies: 79 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):73,881,272-73,881,715Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6916016Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1174,170,22774,170,670
    nsv6916016RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1173,881,27273,881,715

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18352612deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18352612Submitted genomicNC_000011.10:g.741
    70227_74170670del
    GRCh38 (hg38)NC_000011.10Chr1174,170,22774,170,670
    nssv18352612RemappedPerfectNC_000011.9:g.7388
    1272_73881715del
    GRCh37.p13First PassNC_000011.9Chr1173,881,27273,881,715

    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)
    nssv18352612<0.001127262090
    Support Center