A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10493n54



Internal ID22778388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32473615..32539789hg38UCSC Ensembl
chr6:32441392..32507566hg19UCSC Ensembl
chr6:32549370..32615544hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3866175
hg1966175
hg1866175
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602144, nsv602137, nsv602136, nsv602147, nsv602132
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10493n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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