A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3716548



Internal ID19014829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20235273..20404354hg38UCSC Ensembl
Innerchr15:20440526..20609607hg19UCSC Ensembl
Innerchr15:18700540..18869621hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38169082
hg19169082
hg18169082
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052991
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)nssv3716548
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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