A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1947n54



Internal ID22769842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55936174..55962275hg38UCSC Ensembl
chr11:55703650..55729751hg19UCSC Ensembl
chr11:55460226..55486327hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3826102
hg1926102
hg1826102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555091, nsv555090, nsv555088, nsv555094, nsv555092
Samples1782681076_A, 1780854261_A
Known GenesOR5I1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1947n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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