A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935409



Internal ID22710750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:39465306..39466539hg38UCSC Ensembl
chr12:39859108..39860341hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg381234
hg191234
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360351
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935409
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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