A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17399052



Internal ID22456922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39990369..39992487hg38UCSC Ensembl
chr22:40386373..40388491hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg382119
hg192119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961258
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17399052
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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