A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596835



Internal ID6984149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:85340598..85430808hg38UCSC Ensembl
chr3:85389748..85479958hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3890211
hg1990211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11061858, essv11061857
SamplesHG02154, HG02095
Known GenesCADM2, MIR5688
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596835
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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