A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17859316



Internal ID22042959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20267021..20267021hg38UCSC Ensembl
chr6:20267252..20267252hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6260585
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17859316
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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