A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4014873



Internal ID22076504
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155736
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4014873
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer