A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556332



Internal ID329471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117487588..117488295hg38UCSC Ensembl
chr9:120249866..120250573hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38708
hg19708
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028508
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556332
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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