A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295034



Internal ID20504252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98825720..98825787hg38UCSC Ensembl
chr8:99837948..99838015hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743718
Supporting Variants
Samples
Known GenesSTK3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295034
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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