A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14268521



Internal ID6823740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105573551..105595037hg38UCSC Ensembl
chr11:105444278..105465764hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3821487
hg1921487
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627614
Supporting Variants
SamplesNA20901
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14268521
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