A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11187882



Internal ID5151786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152686953..152774079hg38UCSC Ensembl
chr3:152404742..152491868hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3887127
hg1987127
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598212
Supporting Variants
SamplesNA18579
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11187882
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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