A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634588



Internal ID7021391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55993936..56015529hg38UCSC Ensembl
chr14:56460654..56482247hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3821594
hg1921594
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15022291, essv15022290
SamplesHG03693, NA18525
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634588
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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