A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3545671



Internal ID18843952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28465092..28724519hg38UCSC Ensembl
Innerchr15:28710238..28969665hg19UCSC Ensembl
Innerchr15:26499332..26768706hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38259428
hg19259428
hg18269375
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042040
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)nssv3545671
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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