A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093559



Internal ID20660599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119977301..119979200hg38UCSC Ensembl
chr3:119696148..119698047hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369775
Supporting Variants
Samples
Known GenesGSK3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093559
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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