A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv897e214



Internal ID22756791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61895408..61976919hg38UCSC Ensembl
chr3:61881082..61962593hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3881512
hg1981512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3596364, esv3596366
SamplesHG02811, HG02019
Known GenesPTPRG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv897e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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