A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597385



Internal ID6984613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111073649..111077426hg38UCSC Ensembl
chr3:110792496..110796273hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg383778
hg193778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11099854, essv11099852, essv11099851, essv11099853
SamplesHG03018, NA19238, NA19328, HG00672
Known GenesPVRL3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597385
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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