A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998642



Internal ID21907985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:85515014..85515130hg38UCSC Ensembl
chr4:86436167..86436283hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540658
Samples
Known GenesARHGAP24
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998642
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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