A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv382e214



Internal ID22756276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21581135..21590732hg38UCSC Ensembl
chr14:22049269..22058851hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg389598
hg199583
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3633725, esv3633724
SamplesHG03366, HG02433, HG03517, HG02891, HG02870, HG03280, HG03518, HG02285, NA18510, HG02769, NA19171, NA19379, HG03099, HG03135, HG02485, HG02573, NA19238, NA19159, NA19239, HG02977, NA19247, HG03547, HG02307, NA18853, HG03391, HG02255, HG02667, HG03240, NA19256, HG01958, HG02837, NA19144, HG02558, NA20348, HG02851, HG03118, NA19429
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv382e214
Frequency
Sample Size2504
Observed Gain37
Observed Loss0
Observed Complex0
Frequencyn/a


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