A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080559



Internal ID21511626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112150922..112151023hg38UCSC Ensembl
chr13:112805236..112805337hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602029
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080559
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer