A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128081



Internal ID21482276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9822721..9822721hg38UCSC Ensembl
chr3:9864405..9864405hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610578
Supporting Variants
SamplesHG03732
Known GenesARPC4-TTLL3, TTLL3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128081
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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