A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17124000



Internal ID21511236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24757659..24757659hg38UCSC Ensembl
chr22:25153626..25153626hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666751
Supporting Variants
SamplesNA24385
Known GenesPIWIL3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17124000
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