A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859682



Internal ID22634617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46587582..46594146hg38UCSC Ensembl
chr12:46981365..46987929hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg386565
hg196565
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459334
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859682
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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