A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2760372



Internal ID10027735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58429248..58438954hg38UCSC Ensembl
Innerchr15:58721447..58731153hg19UCSC Ensembl
Innerchr15:56508739..56518445hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg389707
hg199707
hg189707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7023340, essv7023339
SamplesRW_0636, RW_0093
Known GenesLIPC
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)esv2760372
Frequency
Sample Size1109
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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