A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197762



Internal ID20764802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34722054..34727444hg38UCSC Ensembl
chr19:35212959..35218349hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg385391
hg195391
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522867
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197762
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