A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6998990



Internal ID10354330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106117522..106372206hg38UCSC Ensembl
Innerchr14:106574118..106828137hg19UCSC Ensembl
Innerchr14:105645163..105899182hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38254685
hg19254020
hg18254020
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2761366
Supporting Variants
SamplesSW_0169
Known GenesLINC00226
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)essv6998990
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