A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374621



Internal ID21032174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133480395..133495862hg38UCSC Ensembl
chr3:133199239..133214706hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3815468
hg1915468
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208988
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374621
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