A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17859774



Internal ID22043417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105879990..105879990hg38UCSC Ensembl
chr6:106327865..106327865hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6256980
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17859774
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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