A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3732606



Internal ID19030887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18279710..18366814hg38UCSC Ensembl
Innerchr21:19652027..19739131hg19UCSC Ensembl
Innerchr21:18573898..18661002hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3887105
hg1987105
hg1887105
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062977
Supporting Variants
Samples
Known GenesTMPRSS15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3732606
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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