A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436591



Internal ID215204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184099468..184101467hg38UCSC Ensembl
chr3:183817256..183819255hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16943309
Samples
Known GenesHTR3E
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436591
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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