A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7003446



Internal ID10020027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42764471..43092819hg38UCSC Ensembl
Innerchr19:43268623..43596971hg19UCSC Ensembl
Innerchr19:47960463..48288811hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38328349
hg19328349
hg18328349
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2763121
Supporting Variants
SamplesSW_1193
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG2, PSG6, PSG7, PSG8
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)essv7003446
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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