A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3600119



Internal ID18898400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:31474270..31536330hg38UCSC Ensembl
Innerchr21:32846583..32908643hg19UCSC Ensembl
Innerchr21:31768454..31830514hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3862061
hg1962061
hg1862061
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061254
Supporting Variants
Samples
Known GenesTIAM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3600119
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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