A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750240



Internal ID20526276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97614413..97616978hg38UCSC Ensembl
chr9:100376695..100379260hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg382566
hg192566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287062
Samples
Known GenesTSTD2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750240
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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