A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4035n54



Internal ID22771930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105738701..105739931hg38UCSC Ensembl
chr14:106205038..106206268hg19UCSC Ensembl
chr14:105276083..105277313hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg381231
hg191231
hg181231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566452, nsv566450, nsv566449, nsv566444, nsv566447, nsv566453
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4035n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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