A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17408649



Internal ID22466519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36455643..36456859hg38UCSC Ensembl
chr22:36851690..36852906hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg381217
hg191217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5960035
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17408649
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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