A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925477



Internal ID22700704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:16389636..16415183hg38UCSC Ensembl
chr12:16542570..16568117hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3825548
hg1925548
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359098
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925477
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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