A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5715089



Internal ID9106766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65690943..65691527hg38UCSC Ensembl
chr14:66157661..66158245hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38585
hg19585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677649
Supporting Variants
SamplesHG01101
Known GenesFUT8
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5715089
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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