A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6260636



Internal ID22065246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25169820..25169820hg38UCSC Ensembl
chr6:25170048..25170048hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17859125
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6260636
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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