A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045455



Internal ID18787986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41244426..41328336hg38UCSC Ensembl
Innerchr15:41536624..41620534hg19UCSC Ensembl
Innerchr15:39323916..39407826hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3883911
hg1983911
hg1883911
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552254
Samples
Known GenesCHP1, OIP5, OIP5-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045455
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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