A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3536965



Internal ID18835246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..20688370hg38UCSC Ensembl
Innerchr15:20216943..20893699hg19UCSC Ensembl
Innerchr15:18476957..19153713hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38676681
hg19676757
hg18676757
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035876
Supporting Variants
Samples
Known GenesCHEK2P2, GOLGA6L6, GOLGA8CP, HERC2P3, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3536965
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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