A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623688



Internal ID7010544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67575998..67696613hg38UCSC Ensembl
chr10:69335756..69456371hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38120616
hg19120616
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13846277, essv13846282, essv13846279, essv13846280, essv13846278, essv13846276, essv13846281, essv13846283
SamplesNA19397, NA19036, NA19436, NA19375, NA19309, NA19149, NA19019, HG01342
Known GenesCTNNA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623688
Frequency
Sample Size2504
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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