A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937430



Internal ID25680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99674706..99676964hg38UCSC Ensembl
chr3:99393550..99395808hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg382259
hg192259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453655
Supporting Variants
Samples
Known GenesCOL8A1, MIR548G
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937430
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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