A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2239n54



Internal ID22770134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:135007772..135070522hg38UCSC Ensembl
chr11:134877666..134940416hg19UCSC Ensembl
chr11:134382876..134445626hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3862751
hg1962751
hg1862751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556839, nsv556840
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2239n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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