A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14274433



Internal ID4195624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107057010..107231994hg38UCSC Ensembl
chr11:106927736..107102720hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38174985
hg19174985
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627641
Supporting Variants
SamplesHG03782
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14274433
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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