A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17684552



Internal ID108218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112413406..112414768hg38UCSC Ensembl
chr12:112851210..112852572hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg381363
hg191363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503223
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17684552
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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