A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587705



Internal ID16028428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43739631..43740697hg38UCSC Ensembl
Innerchr21:45159512..45160578hg19UCSC Ensembl
Innerchr21:43983940..43985006hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381067
hg191067
hg181067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7875n54
Supporting Variantsnssv948022, nssv948021
Samples
Known GenesPDXK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587705
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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