A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039963



Internal ID19129182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20283071..22046199hg38UCSC Ensembl
Innerchr15:20488324..22334150hg19UCSC Ensembl
Innerchr15:18748338..19835514hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381763129
hg191845827
hg181087177
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2214n100
Supporting Variantsnssv3536039
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, 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)nsv1039963
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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