A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1990n54



Internal ID22769885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69488959..69530568hg38UCSC Ensembl
chr11:69303727..69345336hg19UCSC Ensembl
chr11:69012908..69054517hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3841610
hg1941610
hg1841610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555322, nsv555321
Samples1780862042_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1990n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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