A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066377



Internal ID18808908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14727124..15122181hg38UCSC Ensembl
Innerchr20:14707770..15102827hg19UCSC Ensembl
Innerchr20:14655770..15050827hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38395058
hg19395058
hg18395058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4257n100
Supporting Variantsnssv3599425
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)nsv1066377
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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