A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586283



Internal ID16373692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54672056..54694876hg38UCSC Ensembl
Innerchr20:53288595..53311415hg19UCSC Ensembl
Innerchr20:52722002..52744822hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3822821
hg1922821
hg1822821
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv941574
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586283
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer