A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014543



Internal ID21923886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13102342..13102449hg38UCSC Ensembl
chr8:12959851..12959958hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570304
Samples
Known GenesDLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014543
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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