A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585476



Internal ID16026199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14757197..14974297hg38UCSC Ensembl
Innerchr20:14737843..14954943hg19UCSC Ensembl
Innerchr20:14685843..14902943hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38217101
hg19217101
hg18217101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7472n54
Supporting Variantsnssv1151209
SamplesHGDP00643
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585476
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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