A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17838395



Internal ID22022038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96053611..96053611hg38UCSC Ensembl
chr7:95682923..95682923hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6239478
Supporting Variants
Samples
Known GenesDYNC1I1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17838395
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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