A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5402192



Internal ID181563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85955345..85955389hg38UCSC Ensembl
chr9:88570260..88570304hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025578
Samples
Known GenesNAA35
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5402192
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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