A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3817n54



Internal ID22771712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:83380429..83427140hg38UCSC Ensembl
chr14:83846773..83893484hg19UCSC Ensembl
chr14:82916526..82963237hg18UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3846712
hg1946712
hg1846712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565371, nsv565370
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3817n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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