A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839719



Internal ID22614654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6138387..6141402hg38UCSC Ensembl
chr4:6140114..6143129hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg383016
hg193016
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496442
Samples
Known GenesJAKMIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839719
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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