A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17856086



Internal ID22039729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89107103..89107103hg38UCSC Ensembl
chr1:89572786..89572786hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6244338
Supporting Variants
Samples
Known GenesGBP2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17856086
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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