A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052131



Internal ID18794662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27932591..28460005hg38UCSC Ensembl
Innerchr15:28177737..28705000hg19UCSC Ensembl
Innerchr15:25851332..26500067hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38527415
hg19527264
hg18648736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3545662
Samples
Known GenesGOLGA8F, GOLGA8G, HERC2, MIR4509-1, MIR4509-2, MIR4509-3, OCA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052131
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer