A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036360



Internal ID18778891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:65333881..65390204hg38UCSC Ensembl
Innerchr15:65626219..65682542hg19UCSC Ensembl
Innerchr15:63413272..63469595hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3856324
hg1956324
hg1856324
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3717953
Samples
Known GenesIGDCC3, IGDCC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036360
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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