A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936799



Internal ID25251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97762558..97776780hg38UCSC Ensembl
chr3:97481402..97495624hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3814223
hg1914223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5441458
Supporting Variants
Samples
Known GenesARL6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936799
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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