A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063838



Internal ID19153057
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 StatusM
Merged Variantsdgv4267n100
Supporting Variantsnssv3599571
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)nsv1063838
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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