A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836269



Internal ID22611204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42073324..42075598hg38UCSC Ensembl
chr3:42114816..42117090hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg382275
hg192275
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836269
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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