A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3552389



Internal ID18503984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:50469213..50744428hg38UCSC Ensembl
Innerchr15:50761410..51036625hg19UCSC Ensembl
Innerchr15:48548702..48823917hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38275216
hg19275216
hg18275216
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054970
Supporting Variants
Samples
Known GenesSPPL2A, TRPM7, USP50, USP8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3552389
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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