A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019692



Internal ID21929035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87057924..87058782hg38UCSC Ensembl
chr9:89672839..89673697hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38859
hg19859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588524
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019692
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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