A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061573



Internal ID19150792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14909985..15016115hg38UCSC Ensembl
Innerchr20:14890631..14996761hg19UCSC Ensembl
Innerchr20:14838631..14944761hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38106131
hg19106131
hg18106131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599606
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)nsv1061573
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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