A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563854



Internal ID336781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116142703..116142703hg38UCSC Ensembl
chr9:118904982..118904982hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg381
hg191
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028398
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563854
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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