A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052363



Internal ID18794894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67705434..67960615hg38UCSC Ensembl
Innerchr11:67472905..67728086hg19UCSC Ensembl
Innerchr11:67229481..67484662hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38255182
hg19255182
hg18255182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1215n100
Supporting Variantsnssv3519189
Samples
Known GenesFAM86C2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052363
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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