A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17112731



Internal ID21480989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24460107..24460107hg38UCSC Ensembl
chr2:24682976..24682976hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604529
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17112731
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