A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415183



Internal ID194443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:67852136..67852187hg38UCSC Ensembl
chr12:68245916..68245967hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17688799
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415183
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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