A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17684189



Internal ID107855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94466482..94474026hg38UCSC Ensembl
chr12:94860258..94867802hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg387545
hg197545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498068
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17684189
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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