A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11682590



Internal ID3866708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:166326184..166348306hg38UCSC Ensembl
chr4:167247336..167269458hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3822123
hg1922123
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603042
Supporting Variants
SamplesHG03511
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11682590
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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