A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586533



Internal ID16373942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62951856..62967222hg38UCSC Ensembl
Innerchr20:61583208..61598574hg19UCSC Ensembl
Innerchr20:61053653..61069019hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3815367
hg1915367
hg1815367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7659n54
Supporting Variantsnssv942287
Samples
Known GenesSLC17A9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586533
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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