A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7742409



Internal ID13896251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37856302..37856303hg38UCSC Ensembl
Innerchr14:37856232..37856373hg38UCSC Ensembl
Outerchr14:37856231..37856374hg38UCSC Ensembl
chr14:38325507..38325508hg19UCSC Ensembl
Innerchr14:38325437..38325578hg19UCSC Ensembl
Outerchr14:38325436..38325579hg19UCSC Ensembl
chr14:37395258..37395259hg18UCSC Ensembl
Innerchr14:37395329..37395188hg18UCSC Ensembl
Outerchr14:37395187..37395330hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38783
hg19783
hg18783
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3303219
Supporting Variants
SamplesNA18520
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7742409
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