A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706348



Internal ID130014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3242091..3336960hg38UCSC Ensembl
chr16:3292091..3386960hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3894870
hg1994870
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559401
Supporting Variants
Samples
Known GenesLINC00921, MEFV, TIGD7, ZNF263, ZNF75A
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706348
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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