A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17684397



Internal ID108063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109924470..109927301hg38UCSC Ensembl
chr12:110362275..110365106hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg382832
hg192832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512901
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17684397
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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