A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859366



Internal ID22634301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3933415..3935614hg38UCSC Ensembl
chr12:4042581..4044780hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv321n209
Supporting Variantsnssv17453506, nssv17455201
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859366
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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