A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936379



Internal ID22711732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110955832..110956301hg38UCSC Ensembl
chr12:111393636..111394105hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936379
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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