A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1420e214



Internal ID22757314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:134910612..134915656hg38UCSC Ensembl
chr8:135922855..135927899hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg385045
hg195045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3618912, esv3618911
SamplesNA20757
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1420e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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