A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625883



Internal ID7012717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33393775..33543080hg38UCSC Ensembl
chr11:33415321..33564626hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38149306
hg19149306
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14085520, essv14085521
SamplesHG04195, HG01974
Known GenesKIAA1549L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625883
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