A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8740805



Internal ID15083850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67795615..67795615hg38UCSC Ensembl
Innerchr14:67795614..67795616hg38UCSC Ensembl
Outerchr14:67795565..67795665hg38UCSC Ensembl
chr14:68262332..68262332hg19UCSC Ensembl
Innerchr14:68262331..68262333hg19UCSC Ensembl
Outerchr14:68262282..68262382hg19UCSC Ensembl
chr14:67332085..67332085hg18UCSC Ensembl
Innerchr14:67332086..67332084hg18UCSC Ensembl
Outerchr14:67332035..67332135hg18UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38858
hg19858
hg18858
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3360565
Supporting Variants
SamplesNA19240
Known GenesZFYVE26
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8740805
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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