A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2762763



Internal ID10375561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:104931067..105206406hg38UCSC Ensembl
Innerchr8:105943295..106218634hg19UCSC Ensembl
Innerchr8:106012471..106287810hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38275340
hg19275340
hg18275340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7017126
SamplesRW_0548
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)esv2762763
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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