A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3737152



Internal ID18688747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14829616..14931732hg38UCSC Ensembl
Innerchr20:14810262..14912378hg19UCSC Ensembl
Innerchr20:14758262..14860378hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38102117
hg19102117
hg18102117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061473
Supporting Variants
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3737152
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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