A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854142



Internal ID22629077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110606863..110611393hg38UCSC Ensembl
chr12:111044668..111049198hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg384531
hg194531
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854142
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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