A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051535



Internal ID18794066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:796542..900929hg38UCSC Ensembl
Innerchr11:796542..900929hg19UCSC Ensembl
Innerchr11:786542..890929hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38104388
hg19104388
hg18104388
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1013n100
Supporting Variantsnssv3514842, nssv3509668
Samples
Known GenesCD151, CHID1, EFCAB4A, PIDD, PNPLA2, POLR2L, RPLP2, SLC25A22, SNORA52, TSPAN4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051535
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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