A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7015467



Internal ID10015306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87575098..87674944hg38UCSC Ensembl
Innerchr2:87874617..87974463hg19UCSC Ensembl
Innerchr2:87655732..87755578hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3899847
hg1999847
hg1899847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2763649
Supporting Variants
SamplesSW_1021
Known GenesMIR4435-1, MIR4435-2
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)essv7015467
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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