A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585429



Internal ID16372838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:12452637..12488857hg38UCSC Ensembl
Innerchr20:12433285..12469505hg19UCSC Ensembl
Innerchr20:12381285..12417505hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3836221
hg1936221
hg1836221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv938030
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585429
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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