A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019118



Internal ID21928461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33289363..33319783hg38UCSC Ensembl
chr8:33146881..33177301hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3830421
hg1930421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564347
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019118
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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