A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498616



Internal ID275606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85718788..85761160hg38UCSC Ensembl
chr11:85429831..85472203hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3842373
hg1942373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049595
Samples
Known GenesSYTL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498616
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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