A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049862



Internal ID101134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89683418..89725252hg38UCSC Ensembl
chr11:89416586..89458420hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3841835
hg1941835
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500797
Supporting Variants
Samples
Known GenesFOLH1B, TRIM77
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049862
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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