A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951497



Internal ID22726857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19551273..19551352hg38UCSC Ensembl
chr22:19538796..19538875hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404398
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951497
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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