A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639293



Internal ID7026076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80881985..80905380hg38UCSC Ensembl
chr16:80915882..80939277hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3823396
hg1923396
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15535498
SamplesHG01670
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639293
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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