U.S. flag

An official website of the United States government

nsv6316096

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,169

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 177 SVs from 30 studies. See in: genome view    
    Submitted genomic171,285,638-171,288,806Question Mark
    Overlapping variant regions from other studies: 180 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):171,254,777-171,257,945Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6316096Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1171,285,638171,288,806
    nsv6316096RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1171,254,777171,257,945

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18053814deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18053814Submitted genomicNC_000001.11:g.171
    285638_171288806de
    l
    GRCh38 (hg38)NC_000001.11Chr1171,285,638171,288,806
    nssv18053814RemappedPerfectNC_000001.10:g.171
    254777_171257945de
    l
    GRCh37.p13First PassNC_000001.10Chr1171,254,777171,257,945

    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)
    nssv18053814<0.001139180
    Support Center