A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892780



Internal ID18836914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7718343..7992872hg38UCSC Ensembl
Outerchr16:7670604..7992872hg38UCSC Ensembl
Innerchr16:7768345..8042874hg19UCSC Ensembl
Outerchr16:7720606..8042874hg19UCSC Ensembl
Innerchr16:7708346..7982875hg18UCSC Ensembl
Outerchr16:7660607..7982875hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38322269
hg19322269
hg18322269
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788217, essv25788215
Samples
Known GenesRBFOX1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892780
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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