A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838023



Internal ID22612958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146193141..146229352hg38UCSC Ensembl
chr4:147114293..147150504hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3836212
hg1936212
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499649
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838023
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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