A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998426



Internal ID21907769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83603674..83603753hg38UCSC Ensembl
chr4:84524827..84524906hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540810
Samples
Known GenesAGPAT9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998426
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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