A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555286



Internal ID328447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90993662..91001151hg38UCSC Ensembl
chr9:93755944..93763433hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg387490
hg197490
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024968
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555286
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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