A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986297



Internal ID58286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106588531..106588582hg38UCSC Ensembl
chr6:107036406..107036457hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5407265
Supporting Variants
Samples
Known GenesRTN4IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986297
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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