A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2159n54



Internal ID20135583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106915897..106918150hg38UCSC Ensembl
chr11:106786623..106788876hg19UCSC Ensembl
chr11:106291833..106294086hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg382254
hg192254
hg182254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556264, nsv556250, nsv556251, nsv556269, nsv556258, nsv556257
Samples
Known GenesGUCY1A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2159n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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