A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541426



Internal ID21865781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155791233..155791321hg38UCSC Ensembl
chr4:156712385..156712473hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5995502
Supporting Variants
Samples
Known GenesGUCY1B3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541426
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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