A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16959166



Internal ID40091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:171901499..171901538hg38UCSC Ensembl
chr4:172822650..172822689hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5543364
Supporting Variants
Samples
Known GenesGALNTL6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16959166
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000937


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