A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094564



Internal ID20661604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119640731..119691505hg38UCSC Ensembl
chr3:119359578..119410352hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3850775
hg1950775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368772
Supporting Variants
Samples
Known GenesCOX17, POPDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094564
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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