A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211535



Internal ID20778575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181815487..181822142hg38UCSC Ensembl
chr3:181533275..181539930hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg386656
hg196656
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372444
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211535
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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