A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009800



Internal ID21919143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98393104..98393477hg38UCSC Ensembl
chr9:101155386..101155759hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593186
Samples
Known GenesGABBR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009800
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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