A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3538028



Internal ID18836309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20190264..20729850hg38UCSC Ensembl
Innerchr15:20395517..20935179hg19UCSC Ensembl
Innerchr15:18655531..19195186hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38539587
hg19539663
hg18539656
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052006
Supporting Variants
Samples
Known GenesCHEK2P2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3538028
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