A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6257926



Internal ID22062536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95241360..95241360hg38UCSC Ensembl
chr9:98003642..98003642hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17841075
Samples
Known GenesFANCC
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6257926
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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