A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622824



Internal ID7009682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31985116..31996140hg38UCSC Ensembl
chr10:32274044..32285068hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3811025
hg1911025
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13749850
SamplesHG01572
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622824
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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