A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17690642



Internal ID114308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106946171..106951029hg38UCSC Ensembl
chr12:107339949..107344807hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg384859
hg194859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496311
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17690642
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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