A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3547822



Internal ID18499417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32247324..32567645hg38UCSC Ensembl
Innerchr15:32539525..32859846hg19UCSC Ensembl
Innerchr15:30326817..30647138hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38320322
hg19320322
hg18320322
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053723
Supporting Variants
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)nssv3547822
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