A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557638



Internal ID330731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57821146..57915187hg38UCSC Ensembl
chr19:58332514..58426555hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3894042
hg1994042
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724378
Samples
Known GenesFKBP1AP1, ZNF417, ZNF587, ZNF587B, ZNF814
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557638
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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