A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008159



Internal ID21917502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14973806..14979283hg38UCSC Ensembl
chr9:14973804..14979281hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg385478
hg195478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581974
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008159
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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