A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892940



Internal ID18837074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89353948..89396270hg38UCSC Ensembl
Outerchr16:89353948..89396270hg38UCSC Ensembl
Innerchr16:89420356..89462678hg19UCSC Ensembl
Outerchr16:89420356..89462678hg19UCSC Ensembl
Innerchr16:87947857..87990179hg18UCSC Ensembl
Outerchr16:87947857..87990179hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3842323
hg1942323
hg1842323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798082
Samples
Known GenesANKRD11
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892940
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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