A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16976180



Internal ID51519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143221858..143221909hg38UCSC Ensembl
chr5:142601423..142601474hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5399244
Supporting Variants
Samples
Known GenesARHGAP26
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16976180
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004527


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