A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837423



Internal ID22612358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87179480..87191265hg38UCSC Ensembl
chr3:87228630..87240415hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg3811786
hg1911786
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496154
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837423
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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