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nsv6316445

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,262

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 146 SVs from 23 studies. See in: genome view    
    Submitted genomic177,277,131-177,278,392Question Mark
    Overlapping variant regions from other studies: 148 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):177,246,267-177,247,528Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6316445Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1177,277,131177,278,392
    nsv6316445RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1177,246,267177,247,528

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18053784deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18053784Submitted genomicNC_000001.11:g.177
    277131_177278392de
    l
    GRCh38 (hg38)NC_000001.11Chr1177,277,131177,278,392
    nssv18053784RemappedPerfectNC_000001.10:g.177
    246267_177247528de
    l
    GRCh37.p13First PassNC_000001.10Chr1177,246,267177,247,528

    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)
    nssv18053784<0.001137508
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