A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7003078



Internal ID10019947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16684955..16721984hg38UCSC Ensembl
Innerchr1:17011450..17048479hg19UCSC Ensembl
Innerchr1:16884037..16921066hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3837030
hg1937030
hg1837030
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2763736
Supporting Variants
SamplesSW_1190
Known GenesESPNP
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)essv7003078
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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