A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639580



Internal ID6679671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89428666..89441505hg38UCSC Ensembl
Innerchr16:89428666..89441505hg38UCSC Ensembl
Outerchr16:89428329..89441844hg38UCSC Ensembl
chr16:89495074..89507913hg19UCSC Ensembl
Innerchr16:89495074..89507913hg19UCSC Ensembl
Outerchr16:89494737..89508252hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3812840
hg1912840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv555e214
Supporting Variantsessv15569818
SamplesHG01798
Known GenesANKRD11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639580
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