A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5418843



Internal ID197999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101855869..101861372hg38UCSC Ensembl
chr1:102321425..102326928hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg385504
hg195504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16906596
Samples
Known GenesOLFM3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5418843
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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