A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5553927



Internal ID327125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18625931..18663440hg38UCSC Ensembl
chr11:18647478..18684987hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3837510
hg1937510
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044669
Samples
Known GenesSPTY2D1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5553927
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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