A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3734886



Internal ID18686481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14707123..14916956hg38UCSC Ensembl
Innerchr20:14687769..14897602hg19UCSC Ensembl
Innerchr20:14635769..14845602hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38209834
hg19209834
hg18209834
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064226
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)nssv3734886
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer