A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577733



Internal ID21769776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6486648..6486648hg38UCSC Ensembl
chr9:6486648..6486648hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6099859
Supporting Variants
Samples
Known GenesUHRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577733
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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