A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7023829



Internal ID9996056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32837577..33045427hg38UCSC Ensembl
Innerchr16:32848898..33056748hg19UCSC Ensembl
Innerchr16:32756399..32964249hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38207851
hg19207851
hg18207851
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2760413
Supporting Variants
SamplesRW_0277
Known GenesSLC6A10P
MethodMerging
AnalysisTwo different algorithms (PennCNV and Birdseye) were applied to detect CNVs. Only congruent CNV events regarding direction of effect that were detected by both algorithms were merged using the outer borders of the event in a first step. In a second step only CNVs that were detected in at least two individuals were merged into a CNVR.
PlatformMerging
Comments
ReferenceVogler_et_al_2010
Pubmed ID21179565
Accession Number(s)essv7023829
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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