A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093238



Internal ID21438651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26417384..26417384hg38UCSC Ensembl
chr15:26662531..26662531hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664094
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093238
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