A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13842176



Internal ID5286735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:66019702..66211244hg38UCSC Ensembl
chr10:67779460..67971002hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38191543
hg19191543
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623585
Supporting Variants
SamplesNA18740
Known GenesCTNNA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13842176
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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