A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954692



Internal ID22729927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35439075..35439466hg38UCSC Ensembl
chr22:35835068..35835459hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397728
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954692
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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