A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv619e214



Internal ID22756513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61469711..61485339hg38UCSC Ensembl
chr18:59136944..59152572hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3815629
hg1915629
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3642730, esv3642731
SamplesNA20289, NA19213
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv619e214
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer