A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3540017



Internal ID18838298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20078801..20376190hg38UCSC Ensembl
Innerchr15:20284054..20581443hg19UCSC Ensembl
Innerchr15:18544068..18841457hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38297390
hg19297390
hg18297390
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055053
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)nssv3540017
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