A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616909



Internal ID7003795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37567859..37619345hg38UCSC Ensembl
chr8:37425377..37476863hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3851487
hg1951487
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13168741
SamplesNA11931
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616909
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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