A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556411



Internal ID328479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96506175..96507025hg38UCSC Ensembl
chr14:96972512..96973362hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38851
hg19851
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698697
Samples
Known GenesPAPOLA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556411
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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