A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5553662



Internal ID326890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133255280..133255282hg38UCSC Ensembl
chr9:136130667..136130669hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030066
Samples
Known GenesABO
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5553662
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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