A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7008076



Internal ID10002959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:131271344..131326276hg38UCSC Ensembl
Innerchr2:132028917..132083849hg19UCSC Ensembl
Innerchr2:131745387..131800319hg18UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg3854933
hg1954933
hg1854933
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2760576
Supporting Variants
SamplesRW_0619
Known GenesLOC440910
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)essv7008076
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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