A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277842



Internal ID20487060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89010259..89012975hg38UCSC Ensembl
chr1:89475942..89478658hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg382717
hg192717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738882
Supporting Variants
Samples
Known GenesGBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277842
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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