A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839549



Internal ID22614484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3288475..3294830hg38UCSC Ensembl
chr4:3290202..3296557hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg386356
hg196356
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493514
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839549
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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