A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018907



Internal ID21928250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115064475..115064608hg38UCSC Ensembl
chr8:116076704..116076837hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593294
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018907
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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