A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092321



Internal ID22001554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90146191..90146191hg38UCSC Ensembl
chr9:92908473..92908473hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578280
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092321
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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