A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835199



Internal ID22610134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196592241..196595183hg38UCSC Ensembl
chr3:196319112..196322054hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382943
hg192943
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489904
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835199
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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