A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272268



Internal ID20481486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95202331..95202331hg38UCSC Ensembl
chr9:97964613..97964613hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752984
Supporting Variants
Samples
Known GenesFANCC
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272268
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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