A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843088



Internal ID22026731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96444239..96444239hg38UCSC Ensembl
chr11:96177403..96177403hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248367
Supporting Variants
Samples
Known GenesJRKL-AS1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843088
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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