A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155736



Internal ID22086241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:30941701..31000700hg38UCSC Ensembl
Outerchr21:30941013..31002076hg38UCSC Ensembl
Innerchr21:32314020..32373019hg19UCSC Ensembl
Outerchr21:32313332..32374395hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3861064
hg1961064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014873
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155736
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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