A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16930406



Internal ID21012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28248889..28248981hg38UCSC Ensembl
chr3:28290380..28290472hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446324
Supporting Variants
Samples
Known GenesCMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16930406
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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