A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv781e214



Internal ID22756675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38184316..38200199hg38UCSC Ensembl
chr20:36812718..36828601hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3815884
hg1915884
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3645773, esv3645772
SamplesHG00629, NA21086, NA19711
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv781e214
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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