A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7023768



Internal ID9991274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32113010..32868463hg38UCSC Ensembl
Innerchr16:32124331..32879784hg19UCSC Ensembl
Innerchr16:32031832..32787285hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38755454
hg19755454
hg18755454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2760413
Supporting Variants
SamplesRW_0170
Known GenesHERC2P4, LOC390705, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
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)essv7023768
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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