A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599610



Internal ID18551205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14925880..14979454hg38UCSC Ensembl
Innerchr20:14906526..14960100hg19UCSC Ensembl
Innerchr20:14854526..14908100hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3853575
hg1953575
hg1853575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062237
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)nssv3599610
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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