A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11287092



Internal ID5362058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194904602..195019057hg38UCSC Ensembl
chr3:194625331..194739786hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38114456
hg19114456
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599222
Supporting Variants
SamplesNA18909
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11287092
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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