A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633802



Internal ID7020608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24199680..24205242hg38UCSC Ensembl
Innerchr14:24199680..24205242hg38UCSC Ensembl
Outerchr14:24199180..24205742hg38UCSC Ensembl
chr14:24668886..24674448hg19UCSC Ensembl
Innerchr14:24668886..24674448hg19UCSC Ensembl
Outerchr14:24668386..24674948hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg385563
hg195563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14942273
SamplesHG01846
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633802
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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