A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18091254



Internal ID20658294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:103159500..103160138hg38UCSC Ensembl
chr3:102878344..102878982hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359391
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18091254
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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