A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6997056



Internal ID10022796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:15654433..15720911hg38UCSC Ensembl
Innerchr12:15807367..15873845hg19UCSC Ensembl
Innerchr12:15698634..15765112hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3866479
hg1966479
hg1866479
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2760899
Supporting Variants
SamplesSW_1306
Known GenesEPS8
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)essv6997056
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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