A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587375



Internal ID16374784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33248146..33254349hg38UCSC Ensembl
Innerchr21:34620451..34626654hg19UCSC Ensembl
Innerchr21:33542321..33548524hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg386204
hg196204
hg186204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7814n54
Supporting Variantsnssv946616
Samples
Known GenesIFNAR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587375
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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