A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17123726



Internal ID21418917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33355629..33355779hg38UCSC Ensembl
chr22:33751615..33751765hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588356
Supporting Variants
SamplesHG00731
Known GenesLARGE
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17123726
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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