A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282825



Internal ID20492043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:119168599..119168599hg38UCSC Ensembl
chr9:121930877..121930877hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758179
Supporting Variants
Samples
Known GenesBRINP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282825
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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