A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560333



Internal ID333343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30168689..30264730hg38UCSC Ensembl
chr9:30168687..30264728hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3896042
hg1996042
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17022178
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560333
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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