A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14967588



Internal ID2726741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35355781..35359952hg38UCSC Ensembl
Innerchr14:35355781..35359952hg38UCSC Ensembl
Outerchr14:35355556..35360184hg38UCSC Ensembl
chr14:35824987..35829158hg19UCSC Ensembl
Innerchr14:35824987..35829158hg19UCSC Ensembl
Outerchr14:35824762..35829390hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg384172
hg194172
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634056
Supporting Variants
SamplesHG02399
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14967588
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