A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11187886



Internal ID4351773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152769443..152790542hg38UCSC Ensembl
chr3:152487232..152508331hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3821100
hg1921100
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598215
Supporting Variants
SamplesHG03888
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11187886
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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