A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3952n54



Internal ID20137376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104660017..104734040hg38UCSC Ensembl
chr14:105126354..105200377hg19UCSC Ensembl
chr14:104197399..104271422hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3874024
hg1974024
hg1874024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566050, nsv566049
SamplesNINDS_105
Known GenesADSSL1, INF2, MIR4710
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3952n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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