A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6994372



Internal ID10019954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133074203..133082053hg38UCSC Ensembl
Innerchr9:135949590..135957440hg19UCSC Ensembl
Innerchr9:134939411..134947261hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg387851
hg197851
hg187851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2764128
Supporting Variants
SamplesSW_1190
Known Genes
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)essv6994372
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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