A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2760885



Internal ID10377192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:184260123..184307474hg38UCSC Ensembl
Innerchr4:185181276..185228627hg19UCSC Ensembl
Innerchr4:185418270..185465621hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3847352
hg1947352
hg1847352
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7012349, essv7012350
SamplesRW_0176, RW_0184
Known Genes
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)esv2760885
Frequency
Sample Size1109
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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