A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10517n54



Internal ID22778412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32501123..32521324hg38UCSC Ensembl
chr6:32468900..32489101hg19UCSC Ensembl
chr6:32576878..32597079hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3820202
hg1920202
hg1820202
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602354, nsv602340, nsv602359, nsv602332
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10517n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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