A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787798



Internal ID18816585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89941888..90002650hg38UCSC Ensembl
Innerchr16:90008296..90069058hg19UCSC Ensembl
Innerchr16:88535797..88596559hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3860763
hg1960763
hg1860763
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892941
Supporting Variants
Samples
Known GenesAFG3L1P, CENPBD1, DEF8
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787798
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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