A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7020362



Internal ID10344713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:9423047..9575696hg38UCSC Ensembl
Innerchr12:9575643..9728292hg19UCSC Ensembl
Innerchr12:9466910..9619559hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38152650
hg19152650
hg18152650
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2760270
Supporting Variants
SamplesRW_0349
Known GenesDDX12P
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)essv7020362
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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