A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584945



Internal ID18883226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:47377393..47448400hg38UCSC Ensembl
Innerchr20:46006137..46077144hg19UCSC Ensembl
Innerchr20:45439544..45510551hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3871008
hg1971008
hg1871008
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060129
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584945
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