A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17859152



Internal ID22042795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27631480..27631480hg38UCSC Ensembl
chr6:27599259..27599259hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6260663
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17859152
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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