A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5406411



Internal ID185751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94203879..94203930hg38UCSC Ensembl
chr9:96966161..96966212hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025742
Samples
Known GenesMIRLET7DHG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5406411
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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