A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5442602



Internal ID221024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98132800..98169574hg38UCSC Ensembl
chr3:97851644..97888418hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3836775
hg1936775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16935227
Samples
Known GenesOR5H1, OR5H14, OR5H15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5442602
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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