A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836221



Internal ID22611156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31501691..31520173hg38UCSC Ensembl
chr3:31543183..31561665hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg3818483
hg1918483
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491597
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836221
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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