A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17054389



Internal ID104091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:16631998..16632335hg38UCSC Ensembl
chr12:16784932..16785269hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504823
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17054389
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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