A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093533



Internal ID21447924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88897514..88897514hg38UCSC Ensembl
chr15:89440745..89440745hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660417
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093533
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