A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958808



Internal ID22733867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38762827..38766667hg38UCSC Ensembl
chr22:39158832..39162672hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg383841
hg193841
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17407966
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958808
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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