A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689020



Internal ID15088448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102919262..102921360hg38UCSC Ensembl
Innerchr14:102920262..102920360hg38UCSC Ensembl
Outerchr14:102918262..102922360hg38UCSC Ensembl
chr14:103385599..103387697hg19UCSC Ensembl
Innerchr14:103386599..103386697hg19UCSC Ensembl
Outerchr14:103384599..103388697hg19UCSC Ensembl
chr14:102455352..102457450hg18UCSC Ensembl
Innerchr14:102456352..102456450hg18UCSC Ensembl
Outerchr14:102454352..102458450hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg382099
hg192099
hg182099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3358161
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689020
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