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nsv6335442

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:868

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 154 SVs from 23 studies. See in: genome view    
    Submitted genomic171,526,499-171,527,366Question Mark
    Overlapping variant regions from other studies: 157 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):171,495,638-171,496,505Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6335442Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1171,526,499171,527,366
    nsv6335442RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1171,495,638171,496,505

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18201677duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18201677Submitted genomicNC_000001.11:g.171
    526499_171527366du
    p
    GRCh38 (hg38)NC_000001.11Chr1171,526,499171,527,366
    nssv18201677RemappedPerfectNC_000001.10:g.171
    495638_171496505du
    p
    GRCh37.p13First PassNC_000001.10Chr1171,495,638171,496,505

    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)
    nssv18201677<0.001138742
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