A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559401



Internal ID332435
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 StatusM
Merged Variants
Supporting Variantsnssv17706348
Samples
Known GenesLINC00921, MEFV, TIGD7, ZNF263, ZNF75A
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559401
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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