A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096080



Internal ID20663120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153610902..153613904hg38UCSC Ensembl
chr3:153328691..153331693hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg383003
hg193003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365302
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096080
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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