A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738892



Internal ID20514863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129302771..129305123hg38UCSC Ensembl
chr9:132065050..132067402hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382353
hg192353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738892
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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