A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11026214



Internal ID3201862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61956233..61980028hg38UCSC Ensembl
chr3:61941907..61965702hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3823796
hg1923796
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596368
Supporting Variants
SamplesHG02811
Known GenesPTPRG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11026214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer