A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3941n54



Internal ID22771836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103520468..103523420hg38UCSC Ensembl
chr14:103986805..103989757hg19UCSC Ensembl
chr14:103056558..103059510hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg382953
hg192953
hg182953
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565993, nsv565995
Samples
Known GenesCKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3941n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss3
Observed Complex0
Frequencyn/a


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