A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7003699



Internal ID10009497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54226329..54237443hg38UCSC Ensembl
Innerchr19:54730202..54741319hg19UCSC Ensembl
Innerchr19:59422014..59433131hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3811115
hg1911118
hg1811118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2763032
Supporting Variants
SamplesSW_0353
Known GenesLILRA6
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)essv7003699
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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