A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616867



Internal ID7003753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34848819..34859051hg38UCSC Ensembl
chr8:34706337..34716569hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3810233
hg1910233
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13165845
SamplesHG03212
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616867
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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