A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585427



Internal ID16372836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:11979268..12023465hg38UCSC Ensembl
Innerchr20:11959916..12004113hg19UCSC Ensembl
Innerchr20:11907916..11952113hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3844198
hg1944198
hg1844198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv938028
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585427
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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