A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735650



Internal ID20511594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32504734..32504843hg38UCSC Ensembl
chr9:32504732..32504841hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277091
Samples
Known GenesDDX58
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735650
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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