A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3721473



Internal ID19019754
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 StatusS
Merged Variantsnsv1048161
Supporting Variants
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)nssv3721473
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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