U.S. flag

An official website of the United States government

nsv6333300

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:528

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 141 SVs from 20 studies. See in: genome view    
    Submitted genomic192,349,648-192,350,175Question Mark
    Overlapping variant regions from other studies: 141 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):192,318,778-192,319,305Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6333300Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1192,349,648192,350,175
    nsv6333300RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1192,318,778192,319,305

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18055482deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18055482Submitted genomicNC_000001.11:g.192
    349648_192350175de
    l
    GRCh38 (hg38)NC_000001.11Chr1192,349,648192,350,175
    nssv18055482RemappedPerfectNC_000001.10:g.192
    318778_192319305de
    l
    GRCh37.p13First PassNC_000001.10Chr1192,318,778192,319,305

    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)
    nssv18055482<0.001738058
    Support Center