A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643616



Internal ID6683687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8366946..8383577hg38UCSC Ensembl
chr19:8431830..8448461hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3816632
hg1916632
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15989152, essv15989151
SamplesHG01551, HG03258
Known GenesANGPTL4, RAB11B-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643616
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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