A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643762



Internal ID6683832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15052933..15067870hg38UCSC Ensembl
chr19:15163744..15178681hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3814938
hg1914938
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15999922
SamplesHG01046
Known GenesCASP14
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643762
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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