A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048348



Internal ID20615388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4808107..4814041hg38UCSC Ensembl
chr19:4808119..4814053hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385935
hg195935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525241
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048348
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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