A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586223



Internal ID16373632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53858311..53859343hg38UCSC Ensembl
Innerchr20:52474850..52475882hg19UCSC Ensembl
Innerchr20:51908257..51909289hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg381033
hg191033
hg181033
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv941220, nssv941221
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586223
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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