A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052109



Internal ID19141328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54762047..54926183hg38UCSC Ensembl
Innerchr11:51192870..51357233hg19UCSC Ensembl
Innerchr11:51049446..51213809hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38164137
hg19164364
hg18164364
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1154n100
Supporting Variantsnssv3522048
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052109
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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