A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv779e214



Internal ID20122202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25104610..25367702hg38UCSC Ensembl
chr20:25085246..25348338hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38263093
hg19263093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3645577, esv3645575
SamplesHG03135, NA19454
Known GenesABHD12, ENTPD6, LOC284798, PYGB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv779e214
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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