A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6194815



Internal ID9172218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89419155..89428193hg38UCSC Ensembl
Outerchr16:89419118..89428243hg38UCSC Ensembl
Innerchr16:89485563..89494601hg19UCSC Ensembl
Outerchr16:89485526..89494651hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg389126
hg199126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662057
Supporting Variants
SamplesHG00335
Known GenesANKRD11
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6194815
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