A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13846277



Internal ID5570058
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623688
Supporting Variants
SamplesNA19019
Known GenesCTNNA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13846277
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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