A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5430192



Internal ID209009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41992200..41992251hg38UCSC Ensembl
chr12:42386002..42386053hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17055241
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5430192
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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