A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639511



Internal ID6679603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87320763..87352951hg38UCSC Ensembl
chr16:87354369..87386557hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3832189
hg1932189
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15555131, essv15555130
SamplesHG00610, NA12272
Known GenesFBXO31
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639511
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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