A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099517



Internal ID20666557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186376962..186379014hg38UCSC Ensembl
chr3:186094751..186096803hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg382053
hg192053
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364477
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099517
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.03207


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