A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063702



Internal ID18806233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14888616..14906724hg38UCSC Ensembl
Innerchr20:14869262..14887370hg19UCSC Ensembl
Innerchr20:14817262..14835370hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3818109
hg1918109
hg1818109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599599
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)nsv1063702
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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