A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584503



Internal ID18882784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64066107..64138667hg38UCSC Ensembl
Innerchr20:62697460..62770020hg19UCSC Ensembl
Innerchr20:62167904..62240464hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3872561
hg1972561
hg1872561
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055979
Supporting Variants
Samples
Known GenesC20orf201, MIR6813, NPBWR2, OPRL1, RGS19, TCEA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584503
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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