A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7024906



Internal ID10350964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14071226..14233682hg38UCSC Ensembl
Innerchr18:14071225..14233681hg19UCSC Ensembl
Innerchr18:14061225..14223681hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38162457
hg19162457
hg18162457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2760500
Supporting Variants
SamplesRW_0656
Known GenesANKRD20A5P, ZNF519
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)essv7024906
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