A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072746



Internal ID21408214
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 StatusS
Merged Variantsnsv5601696
Supporting Variants
SamplesHG00512
Known GenesTMPRSS13
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072746
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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