A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15106684



Internal ID6143223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98475041..98574455hg38UCSC Ensembl
chr14:98941378..99040792hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3899415
hg1999415
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635465
Supporting Variants
SamplesNA19678
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15106684
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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