A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053728



Internal ID19142947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20364686..20689298hg38UCSC Ensembl
Innerchr15:20569939..20894627hg19UCSC Ensembl
Innerchr15:18829953..19169035hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38324613
hg19324689
hg18339083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2233n100
Supporting Variantsnssv3537655
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053728
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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