A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3716427



Internal ID19014708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20086048..20614845hg38UCSC Ensembl
Innerchr15:20291301..20820147hg19UCSC Ensembl
Innerchr15:18551315..19080161hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38528798
hg19528847
hg18528847
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037479
Supporting Variants
Samples
Known GenesCHEK2P2, GOLGA6L6, 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)nssv3716427
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