A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1702n54



Internal ID20135126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:24385835..24516078hg38UCSC Ensembl
chr11:24407381..24537624hg19UCSC Ensembl
chr11:24363957..24494200hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38130244
hg19130244
hg18130244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553791, nsv553794
SamplesNINDS_94
Known GenesLUZP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1702n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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