A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584769



Internal ID18536364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37793679..38139909hg38UCSC Ensembl
Innerchr20:36422081..36768311hg19UCSC Ensembl
Innerchr20:35855495..36201725hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38346231
hg19346231
hg18346231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057334
Supporting Variants
Samples
Known GenesCTNNBL1, RPRD1B, TGM2, TTI1, VSTM2L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584769
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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