A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091449



Internal ID22000682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101659560..101659560hg38UCSC Ensembl
chr9:104421842..104421842hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580048
Samples
Known GenesGRIN3A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091449
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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