A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586225



Internal ID16373634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53858408..53859238hg38UCSC Ensembl
Innerchr20:52474947..52475777hg19UCSC Ensembl
Innerchr20:51908354..51909184hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38831
hg19831
hg18831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7606n54
Supporting Variantsnssv941223
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586225
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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