A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954134



Internal ID22729394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38509217..38512879hg38UCSC Ensembl
chr22:38905222..38908884hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg383663
hg193663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392459
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954134
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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