A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv782e214



Internal ID20122205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:42655671..42715083hg38UCSC Ensembl
chr20:41284311..41343723hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3859413
hg1959413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3645870, esv3645869
SamplesNA12004, NA21098, NA19454
Known GenesPTPRT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv782e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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