A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6993260



Internal ID10370492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:93459503..93516484hg38UCSC Ensembl
Innerchr8:94471731..94528712hg19UCSC Ensembl
Innerchr8:94540907..94597888hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3856982
hg1956982
hg1856982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2761449
Supporting Variants
SamplesSW_1358
Known GenesLINC00535
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)essv6993260
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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