A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986298



Internal ID58287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106597561..106601327hg38UCSC Ensembl
chr6:107045436..107049202hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg383767
hg193767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469603
Supporting Variants
Samples
Known GenesRTN4IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986298
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002185


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