A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17859162



Internal ID22042805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28459619..28459619hg38UCSC Ensembl
chr6:28427396..28427396hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6260673
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17859162
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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