A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5405767



Internal ID185109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86149039..86149090hg38UCSC Ensembl
chr9:88763954..88764005hg19UCSC Ensembl
Cytoband9q21.33
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 Variantsnssv17023865
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5405767
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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