A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623680



Internal ID7010536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67288048..67291396hg38UCSC Ensembl
Innerchr10:67288048..67291396hg38UCSC Ensembl
Outerchr10:67287830..67291576hg38UCSC Ensembl
chr10:69047806..69051154hg19UCSC Ensembl
Innerchr10:69047806..69051154hg19UCSC Ensembl
Outerchr10:69047588..69051334hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg383349
hg193349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13845467, essv13845466, essv13845465
SamplesHG04002, HG03091, HG02938
Known GenesCTNNA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623680
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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