A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596354



Internal ID6983671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61804722..61842397hg38UCSC Ensembl
chr3:61790396..61828071hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3837676
hg1937676
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11026177
SamplesHG02127
Known GenesPTPRG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596354
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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