A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845340



Internal ID22028983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132676789..132676789hg38UCSC Ensembl
chr11:132546684..132546684hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258512
Supporting Variants
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845340
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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