A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13680541



Internal ID4863475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3817139..3828976hg38UCSC Ensembl
chr10:3859331..3871168hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3811838
hg1911838
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622183
Supporting Variants
SamplesNA12286
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13680541
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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