A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3716426



Internal ID19014707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20086048..20381218hg38UCSC Ensembl
Innerchr15:20291301..20586471hg19UCSC Ensembl
Innerchr15:18551315..18846485hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38295171
hg19295171
hg18295171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047933
Supporting Variants
Samples
Known GenesCHEK2P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3716426
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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