A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6999876



Internal ID10011700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31719286..32151995hg38UCSC Ensembl
Innerchr15:32011489..32444196hg19UCSC Ensembl
Innerchr15:29798781..30231488hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38432710
hg19432708
hg18432708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2761877
Supporting Variants
SamplesSW_0650
Known GenesCHRNA7
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)essv6999876
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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