A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066778



Internal ID18809309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37849676..37921323hg38UCSC Ensembl
Innerchr20:36478078..36549725hg19UCSC Ensembl
Innerchr20:35911492..35983139hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3871648
hg1971648
hg1871648
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584770
Samples
Known GenesCTNNBL1, VSTM2L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066778
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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