A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585484



Internal ID16026207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14777465..15036594hg38UCSC Ensembl
Innerchr20:14758111..15017240hg19UCSC Ensembl
Innerchr20:14706111..14965240hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38259130
hg19259130
hg18259130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7472n54
Supporting Variantsnssv1151212
SamplesHGDP00372
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585484
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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