A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2762513



Internal ID10375311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:31584237..31589702hg38UCSC Ensembl
Innerchr5:31584344..31589809hg19UCSC Ensembl
Innerchr5:31620101..31625566hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg385466
hg195466
hg185466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7012737
SamplesRW_0258
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)esv2762513
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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