A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10381n54



Internal ID22778276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31306468..31357843hg38UCSC Ensembl
chr6:31274245..31325620hg19UCSC Ensembl
chr6:31382224..31433599hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3851376
hg1951376
hg1851376
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601684, nsv601691, nsv601672, nsv601700, nsv601701, nsv601525, nsv601685, nsv601673, nsv601689, nsv601696, nsv601681, nsv601682, nsv601702, nsv601695, nsv601692, nsv601680, nsv601725, nsv601683, nsv601590
Samples
Known GenesHLA-B, MIR6891
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10381n54
Frequency
Sample Size17421
Observed Gain26
Observed Loss0
Observed Complex0
Frequencyn/a


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