A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279098



Internal ID20488316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143012529..143012529hg38UCSC Ensembl
chr5:142392094..142392094hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766441
Supporting Variants
Samples
Known GenesARHGAP26
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279098
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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