A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052326



Internal ID18794857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34378789..34570510hg38UCSC Ensembl
Innerchr15:34670990..34862711hg19UCSC Ensembl
Innerchr15:32458282..32650003hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38191722
hg19191722
hg18191722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2550n100
Supporting Variantsnssv3547880, nssv3547881
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052326
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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