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nsv6333515

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,222

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 138 SVs from 29 studies. See in: genome view    
    Submitted genomic167,085,155-167,090,376Question Mark
    Overlapping variant regions from other studies: 142 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):167,054,392-167,059,613Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6333515Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1167,085,155167,090,376
    nsv6333515RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1167,054,392167,059,613

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18053542deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18053542Submitted genomicNC_000001.11:g.167
    085155_167090376de
    l
    GRCh38 (hg38)NC_000001.11Chr1167,085,155167,090,376
    nssv18053542RemappedPerfectNC_000001.10:g.167
    054392_167059613de
    l
    GRCh37.p13First PassNC_000001.10Chr1167,054,392167,059,613

    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)
    nssv18053542<0.001139246
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