A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352523



Internal ID21010076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43094594..43096584hg38UCSC Ensembl
chr2:43321732..43323722hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381991
hg191991
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209774
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352523
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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