A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584336



Internal ID18882617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:60987482..61014623hg38UCSC Ensembl
Innerchr20:59562538..59589679hg19UCSC Ensembl
Innerchr20:58995933..59023074hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3827142
hg1927142
hg1827142
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056179
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)nssv3584336
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