A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv896e214



Internal ID22756790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61803567..61906991hg38UCSC Ensembl
chr3:61789241..61892665hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38103425
hg19103425
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3596353, esv3596359
SamplesHG02127
Known GenesPTPRG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv896e214
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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