A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587402



Internal ID16028125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:34073078..34073811hg38UCSC Ensembl
Innerchr21:35445378..35446111hg19UCSC Ensembl
Innerchr21:34367248..34367981hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38734
hg19734
hg18734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7820n54
Supporting Variantsnssv946652
Samples
Known GenesMRPS6, SLC5A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587402
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