A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415927



Internal ID22473797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9809959..9809959hg38UCSC Ensembl
chr3:9851643..9851643hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5955505
Supporting Variants
Samples
Known GenesARPC4-TTLL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415927
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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