A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259965



Internal ID20469183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41893339..41893534hg38UCSC Ensembl
chr19:42397410..42397605hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740379
Supporting Variants
Samples
Known GenesARHGEF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259965
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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