A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7000884



Internal ID10013110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32731968..33829363hg38UCSC Ensembl
Innerchr16:32743289..33631830hg19UCSC Ensembl
Innerchr16:32650790..33539331hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381097396
hg19888542
hg18888542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2762243
Supporting Variants
SamplesSW_0801
Known GenesLOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C
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)essv7000884
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