A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404106



Internal ID22461976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37247146..37252066hg38UCSC Ensembl
chr22:37643186..37648106hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg384921
hg194921
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954918
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404106
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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