A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14295586



Internal ID1417945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121808080..121869186hg38UCSC Ensembl
chr11:121678788..121739894hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3861107
hg1961107
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627928
Supporting Variants
SamplesHG01284
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14295586
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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