A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7023507



Internal ID10348789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85812759..85820680hg38UCSC Ensembl
Innerchr15:86355990..86363911hg19UCSC Ensembl
Innerchr15:84156994..84164915hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg387922
hg197922
hg187922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2760395
Supporting Variants
SamplesRW_0600
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)essv7023507
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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