A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091074



Internal ID22000307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96083227..96083227hg38UCSC Ensembl
chr9:98845509..98845509hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594278
Samples
Known GenesLOC158435
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091074
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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