A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3538348



Internal ID18836629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20056971..20381218hg38UCSC Ensembl
Innerchr15:20262224..20586471hg19UCSC Ensembl
Innerchr15:18522238..18846485hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38324248
hg19324248
hg18324248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050119
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)nssv3538348
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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