A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511762



Internal ID288333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94123302..94368932hg38UCSC Ensembl
chr11:93856468..94102098hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38245631
hg19245631
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049963
Samples
Known GenesFOLR4, PANX1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511762
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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