A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892076



Internal ID19186472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95317959..95583117hg38UCSC Ensembl
Outerchr11:95317959..95583117hg38UCSC Ensembl
Innerchr11:95051123..95316281hg19UCSC Ensembl
Outerchr11:95051123..95316281hg19UCSC Ensembl
Innerchr11:94690771..94955929hg18UCSC Ensembl
Outerchr11:94690771..94955929hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38265159
hg19265159
hg18265159
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788627
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892076
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer