A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891851



Internal ID19186247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:67053508..67087264hg38UCSC Ensembl
Outerchr10:67053508..67087264hg38UCSC Ensembl
Innerchr10:68813266..68847022hg19UCSC Ensembl
Outerchr10:68813266..68847022hg19UCSC Ensembl
Innerchr10:68483272..68517028hg18UCSC Ensembl
Outerchr10:68483272..68517028hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3833757
hg1933757
hg1833757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783671
Samples
Known GenesCTNNA3, LRRTM3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891851
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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