A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2132n54



Internal ID22770027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101527719..101565958hg38UCSC Ensembl
chr11:101398450..101436689hg19UCSC Ensembl
chr11:100903660..100941899hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3838240
hg1938240
hg1838240
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556133, nsv556134, nsv556135
Samples
Known GenesTRPC6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2132n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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