A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843831



Internal ID22027474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32412732..32412732hg38UCSC Ensembl
chr11:32434278..32434278hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247944
Supporting Variants
Samples
Known GenesWT1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843831
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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