A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135800



Internal ID21476210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68242306..68242306hg38UCSC Ensembl
chr4:69108024..69108024hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614793
Supporting Variants
SamplesHG03486
Known GenesTMPRSS11B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135800
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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