A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587477



Internal ID16028200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38856996..39140078hg38UCSC Ensembl
Innerchr21:40228920..40512004hg19UCSC Ensembl
Innerchr21:39150790..39433874hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38283083
hg19283085
hg18283085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946773
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587477
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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