A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5417092



Internal ID196297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89297095..89297393hg38UCSC Ensembl
chr1:89762778..89763076hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16905603
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5417092
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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