A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734140



Internal ID20510074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41894735..41894876hg38UCSC Ensembl
chr19:42398808..42398949hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269472
Samples
Known GenesARHGEF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734140
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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