A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560087



Internal ID333101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5252666..5293997hg38UCSC Ensembl
chr10:5294629..5335960hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3841332
hg1941332
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030501
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560087
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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