A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039619



Internal ID19128838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54554865..54639555hg38UCSC Ensembl
Innerchr11:51479725..51564415hg19UCSC Ensembl
Innerchr11:51336301..51420991hg18UCSC Ensembl
Cytoband11p11.11
Allele length
AssemblyAllele length
hg3884691
hg1984691
hg1884691
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508622
Samples
Known GenesOR4C46
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039619
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