A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17690526



Internal ID114192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104368774..104375354hg38UCSC Ensembl
chr12:104762552..104769132hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg386581
hg196581
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558052
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17690526
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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