A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3536972



Internal ID18835253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..20868199hg38UCSC Ensembl
Innerchr15:20216943..21073528hg19UCSC Ensembl
Innerchr15:18476957..19338186hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38856510
hg19856586
hg18861230
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046895
Supporting Variants
Samples
Known GenesCHEK2P2, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, 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)nssv3536972
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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