A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6995836



Internal ID10364197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25167955..25199466hg38UCSC Ensembl
Innerchr11:25189501..25221012hg19UCSC Ensembl
Innerchr11:25146077..25177588hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3831512
hg1931512
hg1831512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2760599
Supporting Variants
SamplesSW_1097
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)essv6995836
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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