A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7022471



Internal ID9996019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106610265..106615672hg38UCSC Ensembl
Innerchr14:107066275..107071685hg19UCSC Ensembl
Innerchr14:106137320..106142730hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg385408
hg195411
hg185411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2760346
Supporting Variants
SamplesRW_0276
Known Genes
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)essv7022471
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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