A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287623



Internal ID20496841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42439659..42439740hg38UCSC Ensembl
chr21:43859769..43859850hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749792
Supporting Variants
Samples
Known GenesUBASH3A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287623
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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