A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17729913



Internal ID153579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50059129..50069180hg38UCSC Ensembl
chr22:50497558..50507609hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3810052
hg1910052
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535194
Supporting Variants
Samples
Known GenesMLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17729913
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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