A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4014871



Internal ID22076502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:28223940..28305469hg38UCSC Ensembl
Outerchr21:28218191..28309424hg38UCSC Ensembl
Innerchr21:29596259..29677788hg19UCSC Ensembl
Outerchr21:29590510..29681743hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3891234
hg1991234
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155734
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4014871
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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