A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041463



Internal ID18783994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67815528..67849977hg38UCSC Ensembl
Innerchr15:68107866..68142315hg19UCSC Ensembl
Innerchr15:65894920..65929369hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3834450
hg1934450
hg1834450
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553651
Samples
Known GenesSKOR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041463
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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