A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498297



Internal ID22556232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118322666..118325975hg38UCSC Ensembl
chr4:119243821..119247130hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg383310
hg193310
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837860
Supporting Variants
Samples
Known GenesPRSS12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498297
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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