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nsv6363080

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:391

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 117 SVs from 29 studies. See in: genome view    
    Submitted genomic11,070,675-11,071,065Question Mark
    Overlapping variant regions from other studies: 117 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):11,112,361-11,112,751Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6363080Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr311,070,67511,071,065
    nsv6363080RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr311,112,36111,112,751

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18092010deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18092010Submitted genomicNC_000003.12:g.110
    70675_11071065del
    GRCh38 (hg38)NC_000003.12Chr311,070,67511,071,065
    nssv18092010RemappedPerfectNC_000003.11:g.111
    12361_11112751del
    GRCh37.p13First PassNC_000003.11Chr311,112,36111,112,751

    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)
    nssv18092010<0.001233680
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