A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958821



Internal ID39856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155793766..155793796hg38UCSC Ensembl
chr4:156714918..156714948hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552579
Supporting Variants
Samples
Known GenesGUCY1B3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958821
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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