A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009123



Internal ID21918466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:24774484..24774693hg38UCSC Ensembl
chr9:24774482..24774691hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581430
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009123
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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