A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161587



Internal ID21499309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29517614..29517614hg38UCSC Ensembl
chr9:29517612..29517612hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5627876
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161587
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