A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267791



Internal ID20477009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95864067..95864142hg38UCSC Ensembl
chr9:98626349..98626424hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732699
Supporting Variants
Samples
Known GenesLINC00476
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267791
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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