A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6260971



Internal ID22065581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165866419..165866419hg38UCSC Ensembl
chr6:166279907..166279907hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17858066
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6260971
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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