A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044648



Internal ID19133867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28176880..28670916hg38UCSC Ensembl
Innerchr15:28422026..28916062hg19UCSC Ensembl
Innerchr15:26095621..26715103hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38494037
hg19494037
hg18619483
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2491n100
Supporting Variantsnssv3721470
Samples
Known GenesGOLGA8F, GOLGA8G, HERC2, 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)nsv1044648
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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