A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586574



Internal ID16373983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63540866..63547263hg38UCSC Ensembl
Innerchr20:62172219..62178616hg19UCSC Ensembl
Innerchr20:61642663..61649060hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg386398
hg196398
hg186398
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv943752, nssv943753
Samples
Known GenesSRMS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586574
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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