A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011232



Internal ID21920575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87234119..87234187hg38UCSC Ensembl
chr9:89849034..89849102hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590694
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011232
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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