A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601696



Internal ID21550346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117926048..117926163hg38UCSC Ensembl
chr11:117796763..117796878hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072746
SamplesHG00512
Known GenesTMPRSS13
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601696
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