A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7004276



Internal ID10356141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13221914..13765257hg38UCSC Ensembl
Innerchr21:14594235..15137578hg19UCSC Ensembl
Innerchr21:13516106..14059449hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38543344
hg19543344
hg18543344
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2763688
Supporting Variants
SamplesSW_0351
Known GenesLOC100288966, MIR3156-3, MIR8069, POTED
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)essv7004276
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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