A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587706



Internal ID16028429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43739631..43740744hg38UCSC Ensembl
Innerchr21:45159512..45160625hg19UCSC Ensembl
Innerchr21:43983940..43985053hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381114
hg191114
hg181114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7875n54
Supporting Variantsnssv948023
Samples
Known GenesPDXK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587706
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