A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7012942



Internal ID10345377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:101831588..101871185hg38UCSC Ensembl
Innerchr5:101167292..101206889hg19UCSC Ensembl
Innerchr5:101195191..101234788hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3839598
hg1939598
hg1839598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2760962
Supporting Variants
SamplesRW_0508
Known Genes
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)essv7012942
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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