A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132573



Internal ID21490993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47732278..47732278hg38UCSC Ensembl
chr22:48128027..48128027hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666352
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132573
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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