A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584640



Internal ID18536235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:18184227..18520274hg38UCSC Ensembl
Innerchr20:18164871..18500918hg19UCSC Ensembl
Innerchr20:18112871..18448918hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38336048
hg19336048
hg18336048
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062244
Supporting Variants
Samples
Known GenesCSRP2BP, DZANK1, LINC00851, MIR3192, POLR3F, RBBP9, SEC23B, ZNF133
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584640
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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