A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843451



Internal ID22027094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101589731..101589731hg38UCSC Ensembl
chr11:101460462..101460462hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258247
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843451
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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