A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584768



Internal ID18536363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37758210..37839999hg38UCSC Ensembl
Innerchr20:36386612..36468401hg19UCSC Ensembl
Innerchr20:35820026..35901815hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3881790
hg1981790
hg1881790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062415
Supporting Variants
Samples
Known GenesCTNNBL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584768
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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