A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622986



Internal ID7009843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38677444..38713444hg38UCSC Ensembl
chr10:38970575..39006575hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3836001
hg1936001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13757664, essv13757665
SamplesHG01896, NA21113
Known GenesACTR3BP5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622986
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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