A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066764



Internal ID18809295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14850979..14920512hg38UCSC Ensembl
Innerchr20:14831625..14901158hg19UCSC Ensembl
Innerchr20:14779625..14849158hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3869534
hg1969534
hg1869534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599592
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)nsv1066764
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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