A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006860



Internal ID21916203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139463015..139463347hg38UCSC Ensembl
chr8:140475258..140475590hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590485
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006860
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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