A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011123



Internal ID21920466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77798564..77852951hg38UCSC Ensembl
chr8:78710799..78765186hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3854388
hg1954388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594548
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011123
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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