A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634209



Internal ID7021013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:41443912..41512331hg38UCSC Ensembl
Innerchr14:41443912..41512331hg38UCSC Ensembl
Outerchr14:41443412..41512831hg38UCSC Ensembl
chr14:41913115..41981534hg19UCSC Ensembl
Innerchr14:41913115..41981534hg19UCSC Ensembl
Outerchr14:41912615..41982034hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3868420
hg1968420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14986052, essv14986051
SamplesNA18934, HG00125
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634209
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