A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623675



Internal ID7010531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67190370..67279521hg38UCSC Ensembl
Innerchr10:67190370..67279521hg38UCSC Ensembl
Outerchr10:67189870..67280021hg38UCSC Ensembl
chr10:68950128..69039279hg19UCSC Ensembl
Innerchr10:68950128..69039279hg19UCSC Ensembl
Outerchr10:68949628..69039779hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3889152
hg1989152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13845048
SamplesHG04002
Known GenesCTNNA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623675
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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