A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2115n54



Internal ID22770010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99193908..99270364hg38UCSC Ensembl
chr11:99064639..99141095hg19UCSC Ensembl
chr11:98569849..98646305hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3876457
hg1976457
hg1876457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556053, nsv556054
Samples
Known GenesCNTN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2115n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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