A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7024434



Internal ID10018193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3981369..4143917hg38UCSC Ensembl
Innerchr3:4023053..4185601hg19UCSC Ensembl
Innerchr3:3998053..4160601hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38162549
hg19162549
hg18162549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2763711
Supporting Variants
SamplesSW_1118
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)essv7024434
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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