A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883036



Internal ID22658013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3480889..3481073hg38UCSC Ensembl
chr1:3397453..3397637hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374944
Samples
Known GenesARHGEF16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883036
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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