A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891734



Internal ID19186130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:227404..420346hg38UCSC Ensembl
Outerchr10:227404..420346hg38UCSC Ensembl
Innerchr10:273344..466286hg19UCSC Ensembl
Outerchr10:273344..466286hg19UCSC Ensembl
Innerchr10:263344..456286hg18UCSC Ensembl
Outerchr10:263344..456286hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38192943
hg19192943
hg18192943
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792552
Samples
Known GenesDIP2C, ZMYND11
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891734
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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