A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5979341



Internal ID8956745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75924044..75926171hg38UCSC Ensembl
chr14:76390387..76392514hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382128
hg192128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2659565
Supporting Variants
SamplesHG01188
Known GenesTTLL5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5979341
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