A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10532n54



Internal ID22778427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32526013..32530183hg38UCSC Ensembl
chr6:32493790..32497960hg19UCSC Ensembl
chr6:32601768..32605938hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg384171
hg194171
hg184171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602421, nsv602420
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10532n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss36
Observed Complex0
Frequencyn/a


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