A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090147



Internal ID21999380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94125490..94125490hg38UCSC Ensembl
chr9:96887772..96887772hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591259
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090147
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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