A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500797



Internal ID277723
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 StatusM
Merged Variants
Supporting Variantsnssv17049862
Samples
Known GenesFOLH1B, TRIM77
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500797
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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