A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16954062



Internal ID36705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118322561..118325922hg38UCSC Ensembl
chr4:119243716..119247077hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg383362
hg193362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454405
Supporting Variants
Samples
Known GenesPRSS12
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16954062
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00281


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