A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1035n71



Internal ID6318655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17475443..17499547hg19UCSC Ensembl
chr11:17432019..17456123hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv897019, nsv897022
SamplesMS16361, MS23340
Known GenesABCC8
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv1035n71
Frequency
Sample Size6533
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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