A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093918



Internal ID20660958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139004622..139008492hg38UCSC Ensembl
chr3:138723464..138727334hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg383871
hg193871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371777
Supporting Variants
Samples
Known GenesPRR23A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093918
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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