A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834506



Internal ID22609441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10985..13518hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382534
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1417n209
Supporting Variantsnssv17483726, nssv17489176, nssv17489175
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834506
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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