A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5541886



Internal ID8519289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87989681..87989918hg38UCSC Ensembl
chr16:88023287..88023524hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2672889
Supporting Variants
SamplesHG00584
Known GenesBANP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5541886
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