A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050871



Internal ID19140090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20376297..21065709hg38UCSC Ensembl
Innerchr15:20581550..21271038hg19UCSC Ensembl
Innerchr15:18841564..19535697hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38689413
hg19689489
hg18694134
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2237n100
Supporting Variantsnssv3535962
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050871
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