A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038796



Internal ID18781327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:113023134..113056430hg38UCSC Ensembl
Innerchr11:112893856..112927152hg19UCSC Ensembl
Innerchr11:112399066..112432362hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3833297
hg1933297
hg1833297
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3510445
Samples
Known GenesNCAM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038796
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