A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17484350



Internal ID22542258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119321426..119323515hg38UCSC Ensembl
chr3:119040273..119042362hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg382090
hg192090
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834857
Supporting Variants
Samples
Known GenesARHGAP31
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17484350
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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