A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623678



Internal ID7010534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67255422..67320520hg38UCSC Ensembl
chr10:69015180..69080278hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3865099
hg1965099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13845221, essv13845220
SamplesHG04002, NA18988
Known GenesCTNNA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623678
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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