A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210060



Internal ID20777100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81876991..81878766hg38UCSC Ensembl
chr3:81926142..81927917hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg381776
hg191776
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355702
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210060
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