A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3715857



Internal ID19014138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20056971..20773569hg38UCSC Ensembl
Innerchr15:20262224..20978898hg19UCSC Ensembl
Innerchr15:18522238..19238943hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38716599
hg19716675
hg18716706
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040273
Supporting Variants
Samples
Known GenesCHEK2P2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3715857
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