A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940392



Internal ID27645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143285491..143285903hg38UCSC Ensembl
chr3:143004333..143004745hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445417
Supporting Variants
Samples
Known GenesSLC9A9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940392
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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