A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5412227



Internal ID191531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120005155..120005206hg38UCSC Ensembl
chr10:121764667..121764718hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039375
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5412227
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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