A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728837



Internal ID152503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37466392..37470977hg38UCSC Ensembl
chr22:37862430..37867015hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg384586
hg194586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5537833
Supporting Variants
Samples
Known GenesMFNG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728837
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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