A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638837



Internal ID7025622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64611581..64618228hg38UCSC Ensembl
Innerchr16:64611581..64618228hg38UCSC Ensembl
Outerchr16:64611081..64618728hg38UCSC Ensembl
chr16:64645484..64652131hg19UCSC Ensembl
Innerchr16:64645484..64652131hg19UCSC Ensembl
Outerchr16:64644984..64652631hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg386648
hg196648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15499291
SamplesNA19131
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638837
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