A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892897



Internal ID19183717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77357375..77651793hg38UCSC Ensembl
Outerchr16:77357375..77651793hg38UCSC Ensembl
Innerchr16:77391272..77685690hg19UCSC Ensembl
Outerchr16:77391272..77685690hg19UCSC Ensembl
Innerchr16:75948773..76243191hg18UCSC Ensembl
Outerchr16:75948773..76243191hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38294419
hg19294419
hg18294419
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787778
Samples
Known GenesADAMTS18
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892897
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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