A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16984389



Internal ID56974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63346376..63346376hg38UCSC Ensembl
chr6:64056281..64056281hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5394415
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16984389
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003627


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