A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688670



Internal ID112336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:65262167..65273275hg38UCSC Ensembl
chr12:65655947..65667055hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg3811109
hg1911109
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559373
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688670
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000624


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