A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274076



Internal ID20483294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133255302..133255302hg38UCSC Ensembl
chr9:136130689..136130689hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767290
Supporting Variants
Samples
Known GenesABO
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274076
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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