A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010393



Internal ID21919736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26935244..26946281hg38UCSC Ensembl
chr8:26792761..26803798hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3811038
hg1911038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560821
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010393
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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