A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6260606



Internal ID22065216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22661033..22661033hg38UCSC Ensembl
chr6:22661262..22661262hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17859095
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6260606
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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