A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636990



Internal ID7023784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78822362..78833185hg38UCSC Ensembl
chr15:79114704..79125527hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3810824
hg1910824
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15302006
SamplesHG04161
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636990
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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