A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052390



Internal ID19141609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93163436..93217551hg38UCSC Ensembl
Innerchr15:93706665..93760780hg19UCSC Ensembl
Innerchr15:91507669..91561784hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3854116
hg1954116
hg1854116
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718192
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052390
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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