A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5400113



Internal ID179497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97473318..97473369hg38UCSC Ensembl
chr9:100235600..100235651hg19UCSC Ensembl
Cytoband9q22.33
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 Variantsnssv17027569
Samples
Known GenesTDRD7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5400113
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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