A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7015902



Internal ID9999325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7336299..7482669hg38UCSC Ensembl
Innerchr8:7193821..7340191hg19UCSC Ensembl
Innerchr8:7181231..7327601hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38146371
hg19146371
hg18146371
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2761169
Supporting Variants
SamplesRW_0525
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB106A, DEFB106B, DEFB4B, FAM66B, SPAG11B, USP17L4, ZNF705G
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)essv7015902
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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