A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3538296



Internal ID18836577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20056971..20373156hg38UCSC Ensembl
Innerchr15:20262224..20578409hg19UCSC Ensembl
Innerchr15:18522238..18838423hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38316186
hg19316186
hg18316186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053300
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)nssv3538296
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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