A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288299



Internal ID20497517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161055786..161055862hg38UCSC Ensembl
chr1:161025576..161025652hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738376
Supporting Variants
Samples
Known GenesARHGAP30
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288299
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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