A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7016226



Internal ID10336459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12403418..12505139hg38UCSC Ensembl
Innerchr8:12260927..12362648hg19UCSC Ensembl
Innerchr8:12305298..12407019hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38101722
hg19101722
hg18101722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2761239
Supporting Variants
SamplesRW_0128
Known GenesFAM66A, FAM86B2, FAM90A25P, LOC100506990
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)essv7016226
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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