A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554080



Internal ID327276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70397332..70398715hg38UCSC Ensembl
chr9:73012248..73013631hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg381384
hg191384
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023303
Samples
Known GenesKLF9
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554080
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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