A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013098



Internal ID21922441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75128414..75128479hg38UCSC Ensembl
chr9:77743330..77743395hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589742
Samples
Known GenesOSTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013098
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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