A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958818



Internal ID39854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155717623..155717794hg38UCSC Ensembl
chr4:156638775..156638946hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473801
Supporting Variants
Samples
Known GenesGUCY1A3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958818
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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