A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837219



Internal ID22612154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:91354079..91356381hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382303
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496811, nssv17492142
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837219
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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