A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044444



Internal ID97369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:26169540..26169540hg38UCSC Ensembl
chr11:26191087..26191087hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5405628
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044444
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.032884


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