A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626830



Internal ID7013660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74086951..74092344hg38UCSC Ensembl
chr11:73797996..73803389hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg385394
hg195394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14212834, essv14212835
SamplesHG02187, HG02484
Known GenesC2CD3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626830
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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