A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4013900



Internal ID22075531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:47837153..48032757hg38UCSC Ensembl
Outerchr20:47821121..48035619hg38UCSC Ensembl
Innerchr20:46465897..46661501hg19UCSC Ensembl
Outerchr20:46449865..46664363hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38214499
hg19214499
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155655
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4013900
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