A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2761557



Internal ID10028910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:120530035..120548529hg38UCSC Ensembl
Innerchr9:123292313..123310807hg19UCSC Ensembl
Innerchr9:122332134..122350628hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3818495
hg1918495
hg1818495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6994366
SamplesSW_0592
Known GenesCDK5RAP2
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)esv2761557
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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