A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596358



Internal ID6983675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61812502..61906991hg38UCSC Ensembl
chr3:61798176..61892665hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3894490
hg1994490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11026195
SamplesHG02277
Known GenesPTPRG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596358
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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