A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3536247



Internal ID18834528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20336715..20609659hg38UCSC Ensembl
Innerchr15:20541968..20814965hg19UCSC Ensembl
Innerchr15:18801982..19074979hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38272945
hg19272998
hg18272998
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035976
Supporting Variants
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3536247
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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