A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290829



Internal ID20500047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116812000..116812120hg38UCSC Ensembl
chr8:117824239..117824359hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744907
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290829
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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