A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3338756



Internal ID15185743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20854912..20855010hg38UCSC Ensembl
Innerchr14:20854941..20854979hg38UCSC Ensembl
Outerchr14:20854843..20855079hg38UCSC Ensembl
chr14:21323071..21323169hg19UCSC Ensembl
Innerchr14:21323100..21323138hg19UCSC Ensembl
Outerchr14:21323002..21323238hg19UCSC Ensembl
chr14:20392911..20393009hg18UCSC Ensembl
Innerchr14:20392978..20392940hg18UCSC Ensembl
Outerchr14:20392842..20393078hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38242
hg19242
hg18242
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8964689, essv8964691, essv8964690
SamplesNA19138, NA10847, NA18499
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3338756
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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