A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633713



Internal ID7020520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21374453..21375958hg38UCSC Ensembl
Innerchr14:21374470..21375941hg38UCSC Ensembl
Outerchr14:21374436..21375975hg38UCSC Ensembl
chr14:21842612..21844117hg19UCSC Ensembl
Innerchr14:21842629..21844100hg19UCSC Ensembl
Outerchr14:21842595..21844134hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381506
hg191506
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14928162, essv14928161
SamplesHG02549, HG02938
Known GenesSUPT16H
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633713
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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