A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7000797



Internal ID10025145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32013091..33973618hg38UCSC Ensembl
Innerchr16:32024412..33776085hg19UCSC Ensembl
Innerchr16:31931913..33683586hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381960528
hg191751674
hg181751674
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2762243
Supporting Variants
SamplesSW_1422
Known GenesHERC2P4, LOC390705, RNU6-76P, SLC6A10P, 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)essv7000797
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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