A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7013643



Internal ID10339784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:39099091..39104258hg38UCSC Ensembl
Innerchr6:39066867..39072034hg19UCSC Ensembl
Innerchr6:39174845..39180012hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg385168
hg195168
hg185168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2761050
Supporting Variants
SamplesRW_0208
Known GenesSAYSD1
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)essv7013643
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