A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128658



Internal ID21465876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19084489..19084568hg38UCSC Ensembl
chr22:19072002..19072081hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592852
Supporting Variants
SamplesHG03065
Known GenesDGCR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128658
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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