A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17163771



Internal ID21460597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95139851..95139851hg38UCSC Ensembl
chr9:97902133..97902133hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640416
Supporting Variants
SamplesHG02818
Known GenesFANCC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17163771
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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