A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3539587



Internal ID18837868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20384762..22108290hg38UCSC Ensembl
Innerchr15:20590015..22396241hg19UCSC Ensembl
Innerchr15:18850029..19897605hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381723529
hg191806227
hg181047577
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054314
Supporting Variants
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N4, 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)nssv3539587
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