A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16969633



Internal ID47071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126064657..126064708hg38UCSC Ensembl
chr6:126385803..126385854hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5397161
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16969633
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.005464


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