A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17133923



Internal ID21512745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183660214..183683770hg38UCSC Ensembl
chr3:183378002..183401558hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3823557
hg1923557
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664796
Supporting Variants
Samples
Known GenesKLHL24
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17133923
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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