A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048161



Internal ID19137380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28465092..28708757hg38UCSC Ensembl
Innerchr15:28710238..28953903hg19UCSC Ensembl
Innerchr15:26496042..26752944hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38243666
hg19243666
hg18256903
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2492n100
Supporting Variantsnssv3721473
Samples
Known GenesGOLGA8F, GOLGA8G, GOLGA8M, HERC2P9, MIR4509-1, MIR4509-2, MIR4509-3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048161
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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