A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11069211



Internal ID3263089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89895723..90040227hg38UCSC Ensembl
chr3:89944873..90089377hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38144505
hg19144505
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596980
Supporting Variants
SamplesHG02882
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11069211
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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