A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014558



Internal ID21923901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89484759..89484895hg38UCSC Ensembl
chr9:92099674..92099810hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588416
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014558
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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