A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269472



Internal ID20478690
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 StatusS
Merged Variantsnsv4734140
Supporting Variants
Samples
Known GenesARHGEF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269472
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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