A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003274



Internal ID21912617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:83851126..83872267hg38UCSC Ensembl
chr8:84763361..84784502hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3821142
hg1921142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580330
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003274
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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