A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280356



Internal ID20489574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6486611..6486611hg38UCSC Ensembl
chr9:6486611..6486611hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754185
Supporting Variants
Samples
Known GenesUHRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280356
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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