A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639247



Internal ID7026030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79705289..79710644hg38UCSC Ensembl
Innerchr16:79705301..79710633hg38UCSC Ensembl
Outerchr16:79705278..79710656hg38UCSC Ensembl
chr16:79739186..79744541hg19UCSC Ensembl
Innerchr16:79739198..79744530hg19UCSC Ensembl
Outerchr16:79739175..79744553hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg385356
hg195356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15530919
SamplesHG00099
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639247
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