A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018988



Internal ID21928331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13732295..13854256hg38UCSC Ensembl
chr9:13732294..13854255hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38121962
hg19121962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592589
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018988
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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