A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053688



Internal ID18796219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32217691..32550909hg38UCSC Ensembl
Innerchr15:32509892..32843110hg19UCSC Ensembl
Innerchr15:30297184..30630402hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38333219
hg19333219
hg18333219
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2543n100
Supporting Variantsnssv3547805
Samples
Known GenesGOLGA8K, GOLGA8O, LOC100996255, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053688
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