A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019196



Internal ID21928539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33936031..33936131hg38UCSC Ensembl
chr8:33793549..33793649hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568861
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019196
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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