A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093912



Internal ID21492187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99463129..99463129hg38UCSC Ensembl
chr13:100115383..100115383hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651384
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093912
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