A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733832



Internal ID20509763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38255264..38255412hg38UCSC Ensembl
chr22:38651270..38651418hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288574
Samples
Known GenesTMEM184B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733832
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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