A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074902



Internal ID20641942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37202349..37205626hg38UCSC Ensembl
chr22:37598389..37601666hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg383278
hg193278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536114
Supporting Variants
Samples
Known GenesSSTR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074902
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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