A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17848582



Internal ID22032225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78837130..78837130hg38UCSC Ensembl
chr17:76833212..76833212hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259101
Supporting Variants
Samples
Known GenesUSP36
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17848582
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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