A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051477



Internal ID19140696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20396289..21997806hg38UCSC Ensembl
Innerchr15:20601542..22285757hg19UCSC Ensembl
Innerchr15:18861556..19787121hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381601518
hg191684216
hg18925566
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2250n100
Supporting Variantsnssv3539683, nssv3539681, nssv3714794, nssv3539684, nssv3539680, nssv3539679, nssv3539678, nssv3539682
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, 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)nsv1051477
Frequency
Sample Size11257
Observed Gain6
Observed Loss2
Observed Complex0
Frequencyn/a


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