A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981423



Internal ID21890766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161055788..161055918hg38UCSC Ensembl
chr1:161025578..161025708hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534749
Samples
Known GenesARHGAP30
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981423
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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