A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3537022



Internal ID18835303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..22256018hg38UCSC Ensembl
Innerchr15:20216943..22543969hg19UCSC Ensembl
Innerchr15:18476957..20045333hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382244329
hg192327027
hg181568377
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040745
Supporting Variants
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, 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)nssv3537022
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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