A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555834



Internal ID328983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89394522..89394585hg38UCSC Ensembl
chr10:91154279..91154342hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036415
Samples
Known GenesIFIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555834
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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