A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17163291



Internal ID21456140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99703140..99703140hg38UCSC Ensembl
chr9:102465422..102465422hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634488
Supporting Variants
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17163291
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