A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161856



Internal ID21454199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6486604..6486604hg38UCSC Ensembl
chr9:6486604..6486604hg19UCSC 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 Variantsnsv5627546
Supporting Variants
SamplesHG02011
Known GenesUHRF2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161856
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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