A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11190132



Internal ID3681641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154524714..154676983hg38UCSC Ensembl
chr3:154242503..154394772hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38152270
hg19152270
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598253
Supporting Variants
SamplesHG03280
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11190132
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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