A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093560



Internal ID20660600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119986527..119987404hg38UCSC Ensembl
chr3:119705374..119706251hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38878
hg19878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363115
Supporting Variants
Samples
Known GenesGSK3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093560
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