A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596362



Internal ID6983679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61833732..61870619hg38UCSC Ensembl
chr3:61819406..61856293hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3836888
hg1936888
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11026199
SamplesHG02127
Known GenesPTPRG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596362
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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