A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5397063



Internal ID176473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8336204..8336255hg38UCSC Ensembl
chr10:8378167..8378218hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031395
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5397063
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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