A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585752



Internal ID16373161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25805553..25884215hg38UCSC Ensembl
Innerchr20:25786189..25864851hg19UCSC Ensembl
Innerchr20:25734189..25812851hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3878663
hg1978663
hg1878663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7522n54
Supporting Variantsnssv938980
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585752
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