A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11269541



Internal ID2111385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:191263515..191280402hg38UCSC Ensembl
chr3:190981304..190998191hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3816888
hg1916888
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599098
Supporting Variants
SamplesHG01920
Known GenesUTS2B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11269541
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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