A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039154



Internal ID18781685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27707535..27947424hg38UCSC Ensembl
Innerchr15:27952681..28192570hg19UCSC Ensembl
Innerchr15:25626276..25866165hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38239890
hg19239890
hg18239890
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3545660
Samples
Known GenesOCA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039154
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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