A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635287



Internal ID7022086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89024137..89063647hg38UCSC Ensembl
chr14:89490481..89529991hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3839511
hg1939511
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15093000
SamplesHG01366
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635287
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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