A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586484



Internal ID16027207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62158583..62188341hg38UCSC Ensembl
Innerchr20:60733639..60763397hg19UCSC Ensembl
Innerchr20:60167034..60196792hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3829759
hg1929759
hg1829759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv942115
Samples
Known GenesMTG2, SS18L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586484
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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