A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17690066



Internal ID113732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95797790..95797799hg38UCSC Ensembl
chr12:96191568..96191577hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3810
hg1910
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561438
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17690066
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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