A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559029



Internal ID332075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109866336..109866343hg38UCSC Ensembl
chr12:110304141..110304148hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg388
hg198
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17684391
Samples
Known GenesGLTP
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559029
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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