A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5410772



Internal ID190087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32152338..32152389hg38UCSC Ensembl
chr8:32009854..32009905hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17009352
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5410772
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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