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nsv6389116

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 146 SVs from 37 studies. See in: genome view    
    Submitted genomic75,859,501-75,861,900Question Mark
    Overlapping variant regions from other studies: 146 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):76,780,654-76,783,053Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6389116Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr475,859,50175,861,900
    nsv6389116RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr476,780,65476,783,053

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18120231deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18120231Submitted genomicNC_000004.12:g.758
    59501_75861900del
    GRCh38 (hg38)NC_000004.12Chr475,859,50175,861,900
    nssv18120231RemappedPerfectNC_000004.11:g.767
    80654_76783053del
    GRCh37.p13First PassNC_000004.11Chr476,780,65476,783,053

    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)
    nssv18120231<0.001139122
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