A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289602



Internal ID20498820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22599078..22599466hg38UCSC Ensembl
chr8:22456591..22456979hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732014
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289602
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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