A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2156n54



Internal ID20135580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106914413..106924401hg38UCSC Ensembl
chr11:106785139..106795127hg19UCSC Ensembl
chr11:106290349..106300337hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg389989
hg199989
hg189989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556255, nsv556237, nsv556268, nsv556263, nsv556247
Samples
Known GenesGUCY1A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2156n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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