A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587395



Internal ID16028118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33326701..33332014hg38UCSC Ensembl
Innerchr21:34699006..34704320hg19UCSC Ensembl
Innerchr21:33620876..33626190hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg385314
hg195315
hg185315
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946645
Samples
Known GenesIFNAR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587395
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