A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269010



Internal ID20478228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28985620..28987724hg38UCSC Ensembl
chr8:28843137..28845241hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg382105
hg192105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747593
Supporting Variants
Samples
Known GenesHMBOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269010
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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