A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11093180



Internal ID5453462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104772592..104876141hg38UCSC Ensembl
chr3:104491436..104594985hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38103550
hg19103550
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597264
Supporting Variants
SamplesNA18966
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11093180
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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