A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2174n54



Internal ID22770069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107750812..107800900hg38UCSC Ensembl
chr11:107621538..107671626hg19UCSC Ensembl
chr11:107126748..107176836hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3850089
hg1950089
hg1850089
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556378, nsv556379
Samples
Known GenesSLC35F2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2174n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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