A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090277



Internal ID21999510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93010606..93010606hg38UCSC Ensembl
chr9:95772888..95772888hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596030
Samples
Known GenesFGD3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090277
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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