A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7010556



Internal ID10339415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15758057..15766844hg38UCSC Ensembl
Innerchr4:15759680..15768467hg19UCSC Ensembl
Innerchr4:15368778..15377565hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg388788
hg198788
hg188788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2760884
Supporting Variants
SamplesRW_0200
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)essv7010556
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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