A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10442n54



Internal ID22778337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31356440..31360765hg38UCSC Ensembl
chr6:31324217..31328542hg19UCSC Ensembl
chr6:31432196..31436521hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg384326
hg194326
hg184326
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601830, nsv601831, nsv601832
Samples
Known GenesHLA-B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10442n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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