A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016209



Internal ID21925552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121781762..121782117hg38UCSC Ensembl
chr8:122794002..122794357hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580160
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016209
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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