A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090750



Internal ID21999983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66060674..66060674hg38UCSC Ensembl
chr9:42460650..42460650hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590582
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090750
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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