A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3832n54



Internal ID22771727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85982294..86033755hg38UCSC Ensembl
chr14:86448638..86500099hg19UCSC Ensembl
chr14:85518391..85569852hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3851462
hg1951462
hg1851462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565454, nsv565456, nsv565457, nsv565455
SamplesNINDS_96
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3832n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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