A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6297655



Internal ID8920815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65060426..65060710hg38UCSC Ensembl
chr14:65527144..65527428hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2665422
Supporting Variants
SamplesHG00422
Known GenesCHURC1-FNTB, FNTB, MAX
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6297655
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