A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583823



Internal ID21775866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98825797..98825894hg38UCSC Ensembl
chr8:99838025..99838122hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005728
Supporting Variants
Samples
Known GenesSTK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583823
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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