A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151849



Internal ID21424095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108247879..108247879hg38UCSC Ensembl
chr9:111010159..111010159hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5631786
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151849
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