A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585649



Internal ID16373058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16023675..16086119hg38UCSC Ensembl
Innerchr20:16004320..16066764hg19UCSC Ensembl
Innerchr20:15952320..16014764hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3862445
hg1962445
hg1862445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv938576
Samples
Known GenesMACROD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585649
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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