A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14047702



Internal ID3351637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:21605053..21680917hg38UCSC Ensembl
chr11:21626599..21702463hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3875865
hg1975865
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625585
Supporting Variants
SamplesHG03006
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14047702
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