A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008809



Internal ID21918152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95864368..95864441hg38UCSC Ensembl
chr9:98626650..98626723hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583978
Samples
Known GenesLINC00476
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008809
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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