A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066836



Internal ID21507434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130024602..130024602hg38UCSC Ensembl
chr10:131822866..131822866hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624852
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066836
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