A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16942209



Internal ID28821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155848047..155848115hg38UCSC Ensembl
chr3:155565836..155565904hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448976
Supporting Variants
Samples
Known GenesSLC33A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16942209
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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