A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3731366



Internal ID19029647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:52995010..53026590hg38UCSC Ensembl
Innerchr20:51611549..51643129hg19UCSC Ensembl
Innerchr20:51044956..51076536hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3831581
hg1931581
hg1831581
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064159
Supporting Variants
Samples
Known GenesTSHZ2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3731366
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer