A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597878



Internal ID6638145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:135840563..135999462hg38UCSC Ensembl
chr3:135559405..135718304hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38158900
hg19158900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11156748
SamplesNA18520
Known GenesPPP2R3A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597878
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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