A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589966



Internal ID18888247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:925142..977237hg38UCSC Ensembl
Innerchr20:905785..957880hg19UCSC Ensembl
Innerchr20:853785..905880hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3852096
hg1952096
hg1852096
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067403
Supporting Variants
Samples
Known GenesRSPO4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589966
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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