A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009959



Internal ID21919302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69640911..69640977hg38UCSC Ensembl
chr9:72255827..72255893hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595802
Samples
Known GenesAPBA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009959
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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