A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6999773



Internal ID10012094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24429604..24518572hg38UCSC Ensembl
Innerchr15:24674751..24763719hg19UCSC Ensembl
Innerchr15:22225844..22314812hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3888969
hg1988969
hg1888969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2761710
Supporting Variants
SamplesSW_0675
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)essv6999773
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer