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nsv6788325

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 193 SVs from 32 studies. See in: genome view    
    Submitted genomic6,569,201-6,595,600Question Mark
    Overlapping variant regions from other studies: 193 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):6,569,434-6,595,833Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6788325Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr66,569,2016,595,600
    nsv6788325RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr66,569,4346,595,833

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18716234duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18716234Submitted genomicNC_000006.12:g.656
    9201_6595600dup
    GRCh38 (hg38)NC_000006.12Chr66,569,2016,595,600
    nssv18716234RemappedPerfectNC_000006.11:g.656
    9434_6595833dup
    GRCh37.p13First PassNC_000006.11Chr66,569,4346,595,833

    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)
    nssv187162344e-061274726
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