A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2761895



Internal ID10029245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6527388..6554181hg38UCSC Ensembl
Innerchr16:6577389..6604182hg19UCSC Ensembl
Innerchr16:6517390..6544183hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3826794
hg1926794
hg1826794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7000509
SamplesSW_1000
Known GenesRBFOX1
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)esv2761895
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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