A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854104



Internal ID22629039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98002042..98018182hg38UCSC Ensembl
chr12:98395820..98411960hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3816141
hg1916141
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462593
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854104
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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