A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv808e214



Internal ID22756702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29925721..29951049hg38UCSC Ensembl
chr21:31298039..31323367hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3825329
hg1925329
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3646811, esv3646810
SamplesHG01443, HG03644
Known GenesGRIK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv808e214
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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