A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555444



Internal ID328600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32091139..32093577hg38UCSC Ensembl
chr19:32582045..32584483hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg382439
hg192439
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722798
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555444
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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