A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049143



Internal ID100648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108568332..109107549hg38UCSC Ensembl
chr11:108439059..108978276hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38539218
hg19539218
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563566
Supporting Variants
Samples
Known GenesDDX10, EXPH5
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049143
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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