A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11026209



Internal ID2256475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61895408..61955530hg38UCSC Ensembl
chr3:61881082..61941204hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3860123
hg1960123
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596364
Supporting Variants
SamplesHG02019
Known GenesPTPRG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11026209
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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