A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561289



Internal ID334273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80890920..80891988hg38UCSC Ensembl
chr9:83505835..83506903hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg381069
hg191069
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024574
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561289
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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