A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633768



Internal ID7020574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22859799..22868227hg38UCSC Ensembl
Innerchr14:22860299..22867727hg38UCSC Ensembl
Outerchr14:22858799..22869227hg38UCSC Ensembl
chr14:23329008..23337436hg19UCSC Ensembl
Innerchr14:23329508..23336936hg19UCSC Ensembl
Outerchr14:23328008..23338436hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg388429
hg198429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14935055, essv14935054, essv14935052, essv14935051, essv14935053
SamplesHG03673, HG03730, HG03953, HG03238, NA20908
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633768
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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