A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891852



Internal ID19186248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:67395878..67462712hg38UCSC Ensembl
Outerchr10:67395878..67462712hg38UCSC Ensembl
Innerchr10:69155636..69222470hg19UCSC Ensembl
Outerchr10:69155636..69222470hg19UCSC Ensembl
Innerchr10:68825642..68892476hg18UCSC Ensembl
Outerchr10:68825642..68892476hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3866835
hg1966835
hg1866835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785241
Samples
Known GenesCTNNA3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891852
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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