A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891850



Internal ID19186246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66648103..66920775hg38UCSC Ensembl
Outerchr10:66648103..66920775hg38UCSC Ensembl
Innerchr10:68407861..68680533hg19UCSC Ensembl
Outerchr10:68407861..68680533hg19UCSC Ensembl
Innerchr10:68077867..68350539hg18UCSC Ensembl
Outerchr10:68077867..68350539hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38272673
hg19272673
hg18272673
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780390
Samples
Known GenesCTNNA3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891850
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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