A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7030420



Internal ID10358878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:698256..773453hg38UCSC Ensembl
Innerchr5:698371..773568hg19UCSC Ensembl
Innerchr5:751371..826568hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3875198
hg1975198
hg1875198
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2763887
Supporting Variants
SamplesSW_0690
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)essv7030420
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