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nsv6321379

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:666

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 132 SVs from 17 studies. See in: genome view    
    Submitted genomic183,499,560-183,500,225Question Mark
    Overlapping variant regions from other studies: 134 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):183,468,695-183,469,360Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6321379Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1183,499,560183,500,225
    nsv6321379RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1183,468,695183,469,360

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18054704deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18054704Submitted genomicNC_000001.11:g.183
    499560_183500225de
    l
    GRCh38 (hg38)NC_000001.11Chr1183,499,560183,500,225
    nssv18054704RemappedPerfectNC_000001.10:g.183
    468695_183469360de
    l
    GRCh37.p13First PassNC_000001.10Chr1183,468,695183,469,360

    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)
    nssv18054704<0.001338528
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