A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596346



Internal ID6983663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61594967..61641874hg38UCSC Ensembl
chr3:61580641..61627548hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3846908
hg1946908
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv895e214
Supporting Variantsessv11026137, essv11026138, essv11026136
SamplesNA18969, NA19079, NA18957
Known GenesPTPRG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596346
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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