A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586613



Internal ID16027336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63691346..63702868hg38UCSC Ensembl
Innerchr20:62322699..62334220hg19UCSC Ensembl
Innerchr20:61793143..61804664hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3811523
hg1911522
hg1811522
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7676n54
Supporting Variantsnssv943841
Samples
Known GenesARFRP1, RTEL1, RTEL1-TNFRSF6B, TNFRSF6B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586613
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