A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7022391



Internal ID9987825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106403147..106487827hg38UCSC Ensembl
Innerchr14:106859058..106943834hg19UCSC Ensembl
Innerchr14:105930103..106014879hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3884681
hg1984777
hg1884777
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2760346
Supporting Variants
SamplesRW_0077
Known GenesLINC00221
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)essv7022391
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer