A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014876



Internal ID21924219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28880965..28881173hg38UCSC Ensembl
chr8:28738482..28738690hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564201
Samples
Known GenesINTS9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014876
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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