A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084367



Internal ID21993600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15488804..15488804hg38UCSC Ensembl
chr9:15488802..15488802hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579789
Samples
Known GenesPSIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084367
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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