A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560396



Internal ID333403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221968932..221975823hg38UCSC Ensembl
chr1:222142274..222149165hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg386892
hg196892
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16897282
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560396
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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