A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17122910



Internal ID21500697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37227454..37227454hg38UCSC Ensembl
chr22:37623494..37623494hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665822
Supporting Variants
SamplesNA19239
Known GenesRAC2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17122910
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer