A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043726



Internal ID96877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38499497..38499548hg38UCSC Ensembl
chr11:38521047..38521098hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5413840
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043726
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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