A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081474



Internal ID21990707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95202338..95202338hg38UCSC Ensembl
chr9:97964620..97964620hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591210
Samples
Known GenesFANCC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081474
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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