A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558387



Internal ID331452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42392212..42393057hg38UCSC Ensembl
chr17:40544230..40545075hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38846
hg19846
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724505
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558387
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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