A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748873



Internal ID20524900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72806323..72806380hg38UCSC Ensembl
chr9:75421239..75421296hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278211
Samples
Known GenesTMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748873
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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