A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843078



Internal ID22026721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95769435..95769435hg38UCSC Ensembl
chr11:95502599..95502599hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248357
Supporting Variants
Samples
Known GenesFAM76B
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843078
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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