A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17559837



Internal ID21884192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25363095..25363259hg38UCSC Ensembl
chr6:25363323..25363487hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017999
Supporting Variants
Samples
Known GenesLRRC16A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17559837
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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