A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10366n54



Internal ID22778261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29942973..29946600hg38UCSC Ensembl
chr6:29910750..29914377hg19UCSC Ensembl
chr6:30018729..30022356hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg383628
hg193628
hg183628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601462, nsv601463
Samples
Known GenesHLA-A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10366n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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