A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622680



Internal ID7009538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25898912..25903077hg38UCSC Ensembl
chr10:26187841..26192006hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg384166
hg194166
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13728166, essv13728167
SamplesHG01956, NA20902
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622680
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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