A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892787



Internal ID18836921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8771962..8795676hg38UCSC Ensembl
Outerchr16:8771962..8795770hg38UCSC Ensembl
Innerchr16:8865819..8889533hg19UCSC Ensembl
Outerchr16:8865819..8889627hg19UCSC Ensembl
Innerchr16:8773320..8797034hg18UCSC Ensembl
Outerchr16:8773320..8797128hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3823809
hg1923809
hg1823809
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788196, essv25788344
Samples
Known GenesABAT, TMEM186
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892787
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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