A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260990



Internal ID20470208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98161571..98161628hg38UCSC Ensembl
chr8:99173799..99173856hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749898
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260990
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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