A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152833



Internal ID21443376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98825797..98825893hg38UCSC Ensembl
chr8:99838025..99838121hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577407
Supporting Variants
SamplesHG00732
Known GenesSTK3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152833
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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