A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5398736



Internal ID178131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88478827..88478878hg38UCSC Ensembl
chr9:91093742..91093793hg19UCSC Ensembl
Cytoband9q22.1
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 Variantsnssv17023971
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5398736
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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