A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7762523



Internal ID14777785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21858060..21858061hg38UCSC Ensembl
Innerchr14:21858028..21858093hg38UCSC Ensembl
Outerchr14:21858027..21858094hg38UCSC Ensembl
chr14:22326237..22326238hg19UCSC Ensembl
Innerchr14:22326205..22326270hg19UCSC Ensembl
Outerchr14:22326204..22326271hg19UCSC Ensembl
chr14:21396077..21396078hg18UCSC Ensembl
Innerchr14:21396110..21396045hg18UCSC Ensembl
Outerchr14:21396044..21396111hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38124
hg19124
hg18124
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3303722
Supporting Variants
SamplesNA18980
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7762523
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