A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6172018



Internal ID9427398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47800616..47818219hg38UCSC Ensembl
chr16:47834527..47852130hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3817604
hg1917604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658290
Supporting Variants
SamplesNA18628
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6172018
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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