A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837860



Internal ID22612795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118322666..118325975hg38UCSC Ensembl
chr4:119243821..119247130hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg383310
hg193310
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498297
Samples
Known GenesPRSS12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837860
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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