A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3539480



Internal ID18837761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20235273..22023848hg38UCSC Ensembl
Innerchr15:20440526..22311799hg19UCSC Ensembl
Innerchr15:18700540..19813163hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381788576
hg191871274
hg181112624
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047848
Supporting Variants
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)nssv3539480
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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