A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599571



Internal ID18897852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14816926..14897834hg38UCSC Ensembl
Innerchr20:14797572..14878480hg19UCSC Ensembl
Innerchr20:14745572..14826480hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3880909
hg1980909
hg1880909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063838
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)nssv3599571
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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