A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866091



Internal ID22641026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3904122..3906821hg38UCSC Ensembl
chr12:4013288..4015987hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453335
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866091
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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