A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959073



Internal ID22734118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43339065..43382282hg38UCSC Ensembl
chr22:43735071..43778288hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3843218
hg1943218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392363
Samples
Known GenesSCUBE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959073
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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